A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3711784



Internal ID19010065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63688137..63803827hg38UCSC Ensembl
Innerchr13:64262270..64377960hg19UCSC Ensembl
Innerchr13:63160271..63275961hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38115691
hg19115691
hg18115691
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040776
Supporting Variants
Samples
Known GenesLINC00395, OR7E156P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3711784
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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