A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654889



Internal ID15391541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:111570373..111573636hg38UCSC Ensembl
Innerchr5:110906071..110909333hg19UCSC Ensembl
Innerchr5:110933970..110937232hg18UCSC Ensembl
Innerchr5:110933970..110937232hg17UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg383264
hg193263
hg183263
hg173263
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517462
Supporting Variants
Samples
Known GenesSTARD4-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv654889
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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