A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526618



Internal ID18824899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63688137..63784313hg38UCSC Ensembl
Innerchr13:64262270..64358446hg19UCSC Ensembl
Innerchr13:63160271..63256447hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3896177
hg1996177
hg1896177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039766
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)nssv3526618
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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