A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655669



Internal ID15045635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4211535..4286727hg38UCSC Ensembl
Innerchr3:4253219..4328411hg19UCSC Ensembl
Innerchr3:4228219..4303411hg18UCSC Ensembl
Innerchr3:4228219..4303411hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3875193
hg1975193
hg1875193
hg1775193
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516589
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv655669
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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