A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv652675



Internal ID15389327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:152135395..152137091hg38UCSC Ensembl
Innerchr5:151514956..151516652hg19UCSC Ensembl
Innerchr5:151495149..151496845hg18UCSC Ensembl
Innerchr5:151495149..151496845hg17UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg381697
hg191697
hg181697
hg171697
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)nssv652675
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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