A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526609



Internal ID18824890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63599815..63831177hg38UCSC Ensembl
Innerchr13:64173948..64405310hg19UCSC Ensembl
Innerchr13:63071949..63303311hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38231363
hg19231363
hg18231363
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050067
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)nssv3526609
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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