A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670602



Internal ID15407254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:105047330..105059949hg38UCSC Ensembl
Innerchr11:104918057..104930676hg19UCSC Ensembl
Innerchr11:104423267..104435886hg18UCSC Ensembl
Innerchr11:104423267..104435886hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3812620
hg1912620
hg1812620
hg1712620
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517089
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670602
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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