A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659309



Internal ID15395961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17283258..17296233hg38UCSC Ensembl
Innerchr5:17283367..17296342hg19UCSC Ensembl
Innerchr5:17336367..17349342hg18UCSC Ensembl
Innerchr5:17336367..17349342hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3812976
hg1912976
hg1812976
hg1712976
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515766
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659309
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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