A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703612



Internal ID15440264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:171502430..171534296hg38UCSC Ensembl
Innerchr5:170929434..170961300hg19UCSC Ensembl
Innerchr5:170862039..170893905hg18UCSC Ensembl
Innerchr5:170862039..170893905hg17UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3831867
hg1931867
hg1831867
hg1731867
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527212
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703612
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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