A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053791



Internal ID19143010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..20670977hg38UCSC Ensembl
Innerchr15:20585976..20876306hg19UCSC Ensembl
Innerchr15:18845990..19136320hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38290255
hg19290331
hg18290331
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2231n100
Supporting Variantsnssv3537250, nssv3714635, nssv3714633, nssv3537249, nssv3714634
Samples
Known GenesGOLGA6L6, GOLGA8CP, HERC2P3, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053791
Frequency
Sample Size11257
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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