A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658043



Internal ID15394695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63914889..63939070hg38UCSC Ensembl
Innerchr13:64489022..64513203hg19UCSC Ensembl
Innerchr13:63387023..63411204hg18UCSC Ensembl
Innerchr13:63387023..63411204hg17UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3824182
hg1924182
hg1824182
hg1724182
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516171
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658043
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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