A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526658



Internal ID18824939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63715171..63819987hg38UCSC Ensembl
Innerchr13:64289304..64394120hg19UCSC Ensembl
Innerchr13:63187305..63292121hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38104817
hg19104817
hg18104817
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047233
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)nssv3526658
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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