A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704626



Internal ID15441278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:61601105..61616865hg38UCSC Ensembl
Innerchr13:62175238..62190998hg19UCSC Ensembl
Innerchr13:61073239..61088999hg18UCSC Ensembl
Innerchr13:61073239..61088999hg17UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3815761
hg1915761
hg1815761
hg1715761
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528090
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704626
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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