A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3714771



Internal ID19013052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20384762..20681492hg38UCSC Ensembl
Innerchr15:20590015..20886821hg19UCSC Ensembl
Innerchr15:18850029..19146835hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38296731
hg19296807
hg18296807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054887
Supporting Variants
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)nssv3714771
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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