A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679507



Internal ID15416159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:152135395..152161327hg38UCSC Ensembl
Innerchr5:151514956..151540888hg19UCSC Ensembl
Innerchr5:151495149..151521081hg18UCSC Ensembl
Innerchr5:151495149..151521081hg17UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3825933
hg1925933
hg1825933
hg1725933
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516251
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679507
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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