A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046923



Internal ID19136142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63747736..63845046hg38UCSC Ensembl
Innerchr13:64321869..64419179hg19UCSC Ensembl
Innerchr13:63219870..63317180hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3897311
hg1997311
hg1897311
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1692n100
Supporting Variantsnssv3711809
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046923
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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