A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697284



Internal ID15087250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:111658208..111667124hg38UCSC Ensembl
Innerchr5:110993905..111002821hg19UCSC Ensembl
Innerchr5:111021804..111030720hg18UCSC Ensembl
Innerchr5:111021804..111030720hg17UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg388917
hg198917
hg188917
hg178917
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520213
Supporting Variants
Samples
Known GenesSTARD4-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697284
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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