A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703778



Internal ID15440430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:146955321..146955801hg38UCSC Ensembl
Innerchr3:146673108..146673588hg19UCSC Ensembl
Innerchr3:148155798..148156278hg18UCSC Ensembl
Innerchr3:148155806..148156286hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38481
hg19481
hg18481
hg17481
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516386
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703778
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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