A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052360



Internal ID19141579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63727459..63818110hg38UCSC Ensembl
Innerchr13:64301592..64392243hg19UCSC Ensembl
Innerchr13:63199593..63290244hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3890652
hg1990652
hg1890652
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1689n100
Supporting Variantsnssv3526662, nssv3526661, nssv3526659, nssv3526660
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)nsv1052360
Frequency
Sample Size11257
Observed Gain1
Observed Loss3
Observed Complex0
Frequencyn/a


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