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nsv932782

  • Variant Calls:9
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:94,061

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 517 SVs from 72 studies. See in: genome view    
Remapped(Score: Perfect):14,932,845-15,026,905Question Mark
Overlapping variant regions from other studies: 517 SVs from 72 studies. See in: genome view    
Submitted genomic14,974,844-15,068,904Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv932782RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1014,932,84514,944,56815,015,36115,026,905
nsv932782Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000010.10Chr1014,974,84414,986,56715,057,36015,068,904

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysis
nssv1610663deletion1015Oligo aCGHProbe signal intensity
nssv1610732deletion826Oligo aCGHProbe signal intensity
nssv1611284deletion1261Oligo aCGHProbe signal intensity
nssv1611320deletion885Oligo aCGHProbe signal intensity
nssv1611687deletion699Oligo aCGHProbe signal intensity
nssv1612424deletion799Oligo aCGHProbe signal intensity
nssv1612821deletion1264Oligo aCGHProbe signal intensity
nssv1611796deletion695Oligo aCGHProbe signal intensity
nssv1611684deletion560Oligo aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1610663RemappedPerfectNC_000010.11:g.(14
932839_14944974)_(
14973283_15043963)
del		GRCh38.p12First PassNC_000010.11Chr1014,932,83914,944,97414,973,28315,043,963
nssv1610732RemappedPerfectNC_000010.11:g.(14
932839_14944974)_(
14973283_15043963)
del		GRCh38.p12First PassNC_000010.11Chr1014,932,83914,944,97414,973,28315,043,963
nssv1611284RemappedPerfectNC_000010.11:g.(14
932839_14944974)_(
14973283_15043963)
del		GRCh38.p12First PassNC_000010.11Chr1014,932,83914,944,97414,973,28315,043,963
nssv1611320RemappedPerfectNC_000010.11:g.(14
932839_14944974)_(
14973283_15043963)
del		GRCh38.p12First PassNC_000010.11Chr1014,932,83914,944,97414,973,28315,043,963
nssv1611687RemappedPerfectNC_000010.11:g.(14
932839_14944974)_(
14973283_15043963)
del		GRCh38.p12First PassNC_000010.11Chr1014,932,83914,944,97414,973,28315,043,963
nssv1612424RemappedPerfectNC_000010.11:g.(14
932839_14944974)_(
14973283_15043963)
del		GRCh38.p12First PassNC_000010.11Chr1014,932,83914,944,97414,973,28315,043,963
nssv1612821RemappedPerfectNC_000010.11:g.(14
932839_14944974)_(
14973283_15043963)
del		GRCh38.p12First PassNC_000010.11Chr1014,932,83914,944,97414,973,28315,043,963
nssv1611796RemappedPerfectNC_000010.11:g.(14
935697_14936201)_(
14973283_15043963)
del		GRCh38.p12First PassNC_000010.11Chr1014,935,69714,936,20114,973,28315,043,963
nssv1611684RemappedPerfectNC_000010.11:g.(14
936756_14939606)_(
14973283_15043963)
del		GRCh38.p12First PassNC_000010.11Chr1014,936,75614,939,60614,973,28315,043,963
nssv1610663RemappedPerfectNC_000010.10:g.(14
974838_14986973)_(
15015282_15085962)
del		GRCh37.p13First PassNC_000010.10Chr1014,974,83814,986,97315,015,28215,085,962
nssv1610732RemappedPerfectNC_000010.10:g.(14
974838_14986973)_(
15015282_15085962)
del		GRCh37.p13First PassNC_000010.10Chr1014,974,83814,986,97315,015,28215,085,962
nssv1611284RemappedPerfectNC_000010.10:g.(14
974838_14986973)_(
15015282_15085962)
del		GRCh37.p13First PassNC_000010.10Chr1014,974,83814,986,97315,015,28215,085,962
nssv1611320RemappedPerfectNC_000010.10:g.(14
974838_14986973)_(
15015282_15085962)
del		GRCh37.p13First PassNC_000010.10Chr1014,974,83814,986,97315,015,28215,085,962
nssv1611687RemappedPerfectNC_000010.10:g.(14
974838_14986973)_(
15015282_15085962)
del		GRCh37.p13First PassNC_000010.10Chr1014,974,83814,986,97315,015,28215,085,962
nssv1612424RemappedPerfectNC_000010.10:g.(14
974838_14986973)_(
15015282_15085962)
del		GRCh37.p13First PassNC_000010.10Chr1014,974,83814,986,97315,015,28215,085,962
nssv1612821RemappedPerfectNC_000010.10:g.(14
974838_14986973)_(
15015282_15085962)
del		GRCh37.p13First PassNC_000010.10Chr1014,974,83814,986,97315,015,28215,085,962
nssv1611796RemappedPerfectNC_000010.10:g.(14
977696_14978200)_(
15015282_15085962)
del		GRCh37.p13First PassNC_000010.10Chr1014,977,69614,978,20015,015,28215,085,962
nssv1611684RemappedPerfectNC_000010.10:g.(14
978755_14981605)_(
15015282_15085962)
del		GRCh37.p13First PassNC_000010.10Chr1014,978,75514,981,60515,015,28215,085,962
nssv1610663Submitted genomicNC_000010.9:g.(150
14844_15026979)_(1
5055288_15125968)d
el		NCBI36 (hg18)NC_000010.9Chr1015,014,84415,026,97915,055,28815,125,968
nssv1610732Submitted genomicNC_000010.9:g.(150
14844_15026979)_(1
5055288_15125968)d
el		NCBI36 (hg18)NC_000010.9Chr1015,014,84415,026,97915,055,28815,125,968
nssv1611284Submitted genomicNC_000010.9:g.(150
14844_15026979)_(1
5055288_15125968)d
el		NCBI36 (hg18)NC_000010.9Chr1015,014,84415,026,97915,055,28815,125,968
nssv1611320Submitted genomicNC_000010.9:g.(150
14844_15026979)_(1
5055288_15125968)d
el		NCBI36 (hg18)NC_000010.9Chr1015,014,84415,026,97915,055,28815,125,968
nssv1611687Submitted genomicNC_000010.9:g.(150
14844_15026979)_(1
5055288_15125968)d
el		NCBI36 (hg18)NC_000010.9Chr1015,014,84415,026,97915,055,28815,125,968
nssv1612424Submitted genomicNC_000010.9:g.(150
14844_15026979)_(1
5055288_15125968)d
el		NCBI36 (hg18)NC_000010.9Chr1015,014,84415,026,97915,055,28815,125,968
nssv1612821Submitted genomicNC_000010.9:g.(150
14844_15026979)_(1
5055288_15125968)d
el		NCBI36 (hg18)NC_000010.9Chr1015,014,84415,026,97915,055,28815,125,968
nssv1611796Submitted genomicNC_000010.9:g.(150
17702_15018206)_(1
5055288_15125968)d
el		NCBI36 (hg18)NC_000010.9Chr1015,017,70215,018,20615,055,28815,125,968
nssv1611684Submitted genomicNC_000010.9:g.(150
18761_15021611)_(1
5055288_15125968)d
el		NCBI36 (hg18)NC_000010.9Chr1015,018,76115,021,61115,055,28815,125,968

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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