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nsv1039022

  • Variant Calls:19
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:131,409

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2723 SVs from 97 studies. See in: genome view    
Remapped(Score: Good):20,380,723-20,512,131Question Mark
Overlapping variant regions from other studies: 2725 SVs from 97 studies. See in: genome view    
Remapped(Score: Perfect):20,585,976-20,717,374Question Mark
Overlapping variant regions from other studies: 1521 SVs from 36 studies. See in: genome view    
Submitted genomic18,845,990-18,977,388Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv1039022RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000015.10Chr1520,380,72320,512,131
nsv1039022RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1520,585,97620,717,374
nsv1039022Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000015.8Chr1518,845,99018,977,388

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv3537194copy number lossSNP arrayProbe signal intensity
nssv3537195copy number lossSNP arrayProbe signal intensity
nssv3537196copy number lossSNP arrayProbe signal intensity
nssv3537197copy number gainSNP arrayProbe signal intensity
nssv3537198copy number gainSNP arrayProbe signal intensity
nssv3537199copy number gainSNP arrayProbe signal intensity
nssv3537200copy number lossSNP arrayProbe signal intensity
nssv3537201copy number lossSNP arrayProbe signal intensity
nssv3537202copy number lossSNP arrayProbe signal intensity
nssv3537203copy number lossSNP arrayProbe signal intensity
nssv3537204copy number lossSNP arrayProbe signal intensity
nssv3537205copy number lossSNP arrayProbe signal intensity
nssv3714603copy number gainSNP arrayProbe signal intensity
nssv3714604copy number gainSNP arrayProbe signal intensity
nssv3714605copy number gainSNP arrayProbe signal intensity
nssv3714606copy number lossSNP arrayProbe signal intensity
nssv3714607copy number lossSNP arrayProbe signal intensity
nssv3714608copy number lossSNP arrayProbe signal intensity
nssv3714609copy number lossSNP arrayProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv3537194RemappedGoodNC_000015.10:g.(?_
20380723)_(2051213
1_?)del
GRCh38.p12First PassNC_000015.10Chr1520,380,72320,512,131
nssv3537195RemappedGoodNC_000015.10:g.(?_
20380723)_(2051213
1_?)del
GRCh38.p12First PassNC_000015.10Chr1520,380,72320,512,131
nssv3537196RemappedGoodNC_000015.10:g.(?_
20380723)_(2051213
1_?)del
GRCh38.p12First PassNC_000015.10Chr1520,380,72320,512,131
nssv3537197RemappedGoodNC_000015.10:g.(?_
20380723)_(2051213
1_?)dup
GRCh38.p12First PassNC_000015.10Chr1520,380,72320,512,131
nssv3537198RemappedGoodNC_000015.10:g.(?_
20380723)_(2051213
1_?)dup
GRCh38.p12First PassNC_000015.10Chr1520,380,72320,512,131
nssv3537199RemappedGoodNC_000015.10:g.(?_
20380723)_(2051213
1_?)dup
GRCh38.p12First PassNC_000015.10Chr1520,380,72320,512,131
nssv3537200RemappedGoodNC_000015.10:g.(?_
20380723)_(2051213
1_?)del
GRCh38.p12First PassNC_000015.10Chr1520,380,72320,512,131
nssv3537201RemappedGoodNC_000015.10:g.(?_
20380723)_(2051213
1_?)del
GRCh38.p12First PassNC_000015.10Chr1520,380,72320,512,131
nssv3537202RemappedGoodNC_000015.10:g.(?_
20380723)_(2051213
1_?)del
GRCh38.p12First PassNC_000015.10Chr1520,380,72320,512,131
nssv3537203RemappedGoodNC_000015.10:g.(?_
20380723)_(2051213
1_?)del
GRCh38.p12First PassNC_000015.10Chr1520,380,72320,512,131
nssv3537204RemappedGoodNC_000015.10:g.(?_
20380723)_(2051213
1_?)del
GRCh38.p12First PassNC_000015.10Chr1520,380,72320,512,131
nssv3537205RemappedGoodNC_000015.10:g.(?_
20380723)_(2051213
1_?)del
GRCh38.p12First PassNC_000015.10Chr1520,380,72320,512,131
nssv3714603RemappedGoodNC_000015.10:g.(?_
20380723)_(2051213
1_?)dup
GRCh38.p12First PassNC_000015.10Chr1520,380,72320,512,131
nssv3714604RemappedGoodNC_000015.10:g.(?_
20380723)_(2051213
1_?)dup
GRCh38.p12First PassNC_000015.10Chr1520,380,72320,512,131
nssv3714605RemappedGoodNC_000015.10:g.(?_
20380723)_(2051213
1_?)dup
GRCh38.p12First PassNC_000015.10Chr1520,380,72320,512,131
nssv3714606RemappedGoodNC_000015.10:g.(?_
20380723)_(2051213
1_?)del
GRCh38.p12First PassNC_000015.10Chr1520,380,72320,512,131
nssv3714607RemappedGoodNC_000015.10:g.(?_
20380723)_(2051213
1_?)del
GRCh38.p12First PassNC_000015.10Chr1520,380,72320,512,131
nssv3714608RemappedGoodNC_000015.10:g.(?_
20380723)_(2051213
1_?)del
GRCh38.p12First PassNC_000015.10Chr1520,380,72320,512,131
nssv3714609RemappedGoodNC_000015.10:g.(?_
20380723)_(2051213
1_?)del
GRCh38.p12First PassNC_000015.10Chr1520,380,72320,512,131
nssv3537194RemappedPerfectNC_000015.9:g.(?_2
0585976)_(20717374
_?)del
GRCh37.p13First PassNC_000015.9Chr1520,585,97620,717,374
nssv3537195RemappedPerfectNC_000015.9:g.(?_2
0585976)_(20717374
_?)del
GRCh37.p13First PassNC_000015.9Chr1520,585,97620,717,374
nssv3537196RemappedPerfectNC_000015.9:g.(?_2
0585976)_(20717374
_?)del
GRCh37.p13First PassNC_000015.9Chr1520,585,97620,717,374
nssv3537197RemappedPerfectNC_000015.9:g.(?_2
0585976)_(20717374
_?)dup
GRCh37.p13First PassNC_000015.9Chr1520,585,97620,717,374
nssv3537198RemappedPerfectNC_000015.9:g.(?_2
0585976)_(20717374
_?)dup
GRCh37.p13First PassNC_000015.9Chr1520,585,97620,717,374
nssv3537199RemappedPerfectNC_000015.9:g.(?_2
0585976)_(20717374
_?)dup
GRCh37.p13First PassNC_000015.9Chr1520,585,97620,717,374
nssv3537200RemappedPerfectNC_000015.9:g.(?_2
0585976)_(20717374
_?)del
GRCh37.p13First PassNC_000015.9Chr1520,585,97620,717,374
nssv3537201RemappedPerfectNC_000015.9:g.(?_2
0585976)_(20717374
_?)del
GRCh37.p13First PassNC_000015.9Chr1520,585,97620,717,374
nssv3537202RemappedPerfectNC_000015.9:g.(?_2
0585976)_(20717374
_?)del
GRCh37.p13First PassNC_000015.9Chr1520,585,97620,717,374
nssv3537203RemappedPerfectNC_000015.9:g.(?_2
0585976)_(20717374
_?)del
GRCh37.p13First PassNC_000015.9Chr1520,585,97620,717,374
nssv3537204RemappedPerfectNC_000015.9:g.(?_2
0585976)_(20717374
_?)del
GRCh37.p13First PassNC_000015.9Chr1520,585,97620,717,374
nssv3537205RemappedPerfectNC_000015.9:g.(?_2
0585976)_(20717374
_?)del
GRCh37.p13First PassNC_000015.9Chr1520,585,97620,717,374
nssv3714603RemappedPerfectNC_000015.9:g.(?_2
0585976)_(20717374
_?)dup
GRCh37.p13First PassNC_000015.9Chr1520,585,97620,717,374
nssv3714604RemappedPerfectNC_000015.9:g.(?_2
0585976)_(20717374
_?)dup
GRCh37.p13First PassNC_000015.9Chr1520,585,97620,717,374
nssv3714605RemappedPerfectNC_000015.9:g.(?_2
0585976)_(20717374
_?)dup
GRCh37.p13First PassNC_000015.9Chr1520,585,97620,717,374
nssv3714606RemappedPerfectNC_000015.9:g.(?_2
0585976)_(20717374
_?)del
GRCh37.p13First PassNC_000015.9Chr1520,585,97620,717,374
nssv3714607RemappedPerfectNC_000015.9:g.(?_2
0585976)_(20717374
_?)del
GRCh37.p13First PassNC_000015.9Chr1520,585,97620,717,374
nssv3714608RemappedPerfectNC_000015.9:g.(?_2
0585976)_(20717374
_?)del
GRCh37.p13First PassNC_000015.9Chr1520,585,97620,717,374
nssv3714609RemappedPerfectNC_000015.9:g.(?_2
0585976)_(20717374
_?)del
GRCh37.p13First PassNC_000015.9Chr1520,585,97620,717,374
nssv3537194Submitted genomicNC_000015.8:g.(?_1
8845990)_(18977388
_?)del
NCBI36 (hg18)NC_000015.8Chr1518,845,99018,977,388
nssv3537195Submitted genomicNC_000015.8:g.(?_1
8845990)_(18977388
_?)del
NCBI36 (hg18)NC_000015.8Chr1518,845,99018,977,388
nssv3537196Submitted genomicNC_000015.8:g.(?_1
8845990)_(18977388
_?)del
NCBI36 (hg18)NC_000015.8Chr1518,845,99018,977,388
nssv3537197Submitted genomicNC_000015.8:g.(?_1
8845990)_(18977388
_?)dup
NCBI36 (hg18)NC_000015.8Chr1518,845,99018,977,388
nssv3537198Submitted genomicNC_000015.8:g.(?_1
8845990)_(18977388
_?)dup
NCBI36 (hg18)NC_000015.8Chr1518,845,99018,977,388
nssv3537199Submitted genomicNC_000015.8:g.(?_1
8845990)_(18977388
_?)dup
NCBI36 (hg18)NC_000015.8Chr1518,845,99018,977,388
nssv3537200Submitted genomicNC_000015.8:g.(?_1
8845990)_(18977388
_?)del
NCBI36 (hg18)NC_000015.8Chr1518,845,99018,977,388
nssv3537201Submitted genomicNC_000015.8:g.(?_1
8845990)_(18977388
_?)del
NCBI36 (hg18)NC_000015.8Chr1518,845,99018,977,388
nssv3537202Submitted genomicNC_000015.8:g.(?_1
8845990)_(18977388
_?)del
NCBI36 (hg18)NC_000015.8Chr1518,845,99018,977,388
nssv3537203Submitted genomicNC_000015.8:g.(?_1
8845990)_(18977388
_?)del
NCBI36 (hg18)NC_000015.8Chr1518,845,99018,977,388
nssv3537204Submitted genomicNC_000015.8:g.(?_1
8845990)_(18977388
_?)del
NCBI36 (hg18)NC_000015.8Chr1518,845,99018,977,388
nssv3537205Submitted genomicNC_000015.8:g.(?_1
8845990)_(18977388
_?)del
NCBI36 (hg18)NC_000015.8Chr1518,845,99018,977,388
nssv3714603Submitted genomicNC_000015.8:g.(?_1
8845990)_(18977388
_?)dup
NCBI36 (hg18)NC_000015.8Chr1518,845,99018,977,388
nssv3714604Submitted genomicNC_000015.8:g.(?_1
8845990)_(18977388
_?)dup
NCBI36 (hg18)NC_000015.8Chr1518,845,99018,977,388
nssv3714605Submitted genomicNC_000015.8:g.(?_1
8845990)_(18977388
_?)dup
NCBI36 (hg18)NC_000015.8Chr1518,845,99018,977,388
nssv3714606Submitted genomicNC_000015.8:g.(?_1
8845990)_(18977388
_?)del
NCBI36 (hg18)NC_000015.8Chr1518,845,99018,977,388
nssv3714607Submitted genomicNC_000015.8:g.(?_1
8845990)_(18977388
_?)del
NCBI36 (hg18)NC_000015.8Chr1518,845,99018,977,388
nssv3714608Submitted genomicNC_000015.8:g.(?_1
8845990)_(18977388
_?)del
NCBI36 (hg18)NC_000015.8Chr1518,845,99018,977,388
nssv3714609Submitted genomicNC_000015.8:g.(?_1
8845990)_(18977388
_?)del
NCBI36 (hg18)NC_000015.8Chr1518,845,99018,977,388

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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