A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3711775



Internal ID19010056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63688137..63793857hg38UCSC Ensembl
Innerchr13:64262270..64367990hg19UCSC Ensembl
Innerchr13:63160271..63265991hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38105721
hg19105721
hg18105721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045902
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)nssv3711775
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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