A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047467



Internal ID19136686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63688137..63807391hg38UCSC Ensembl
Innerchr13:64262270..64381524hg19UCSC Ensembl
Innerchr13:63160271..63279525hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38119255
hg19119255
hg18119255
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1686n100
Supporting Variantsnssv3526650
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)nsv1047467
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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