A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699607



Internal ID15436259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:2625719..2641408hg38UCSC Ensembl
Innerchr5:2625833..2641522hg19UCSC Ensembl
Innerchr5:2678833..2694522hg18UCSC Ensembl
Innerchr5:2678833..2694522hg17UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3815690
hg1915690
hg1815690
hg1715690
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523782
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699607
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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