A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695471



Internal ID15432123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:108587485..108588229hg38UCSC Ensembl
Innerchr13:109239833..109240577hg19UCSC Ensembl
Innerchr13:108037834..108038578hg18UCSC Ensembl
Innerchr13:108037834..108038578hg17UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38745
hg19745
hg18745
hg17745
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518060
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695471
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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