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nsv832751

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:210,530

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 607 SVs from 59 studies. See in: genome view    
Remapped(Score: Perfect):25,619,836-25,830,365Question Mark
Overlapping variant regions from other studies: 607 SVs from 59 studies. See in: genome view    
Remapped(Score: Perfect):26,089,042-26,299,571Question Mark
Overlapping variant regions from other studies: 61 SVs from 5 studies. See in: genome view    
Submitted genomic25,158,882-25,369,411Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv832751RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000014.9Chr1425,619,83625,830,365
nsv832751RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1426,089,04226,299,571
nsv832751Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000014.7Chr1425,158,88225,369,411

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv1450900copy number lossBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1450900RemappedPerfectNC_000014.9:g.(256
19836_?)_(?_258303
65)del
GRCh38.p12First PassNC_000014.9Chr1425,619,83625,830,365
nssv1450900RemappedPerfectNC_000014.8:g.(260
89042_?)_(?_262995
71)del
GRCh37.p13First PassNC_000014.8Chr1426,089,04226,299,571
nssv1450900Submitted genomicNC_000014.7:g.(251
58882_?)_(?_253694
11)del
NCBI35 (hg17)NC_000014.7Chr1425,158,88225,369,411

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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