A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695797



Internal ID15432449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:31688574..31696834hg38UCSC Ensembl
Innerchr5:31688681..31696941hg19UCSC Ensembl
Innerchr5:31724438..31732698hg18UCSC Ensembl
Innerchr5:31724438..31732698hg17UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg388261
hg198261
hg188261
hg178261
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518370
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695797
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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