A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699208



Internal ID15089174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:22807060..22847391hg38UCSC Ensembl
Innerchr11:22828606..22868937hg19UCSC Ensembl
Innerchr11:22785182..22825513hg18UCSC Ensembl
Innerchr11:22785182..22825513hg17UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3840332
hg1940332
hg1840332
hg1740332
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523451
Supporting Variants
Samples
Known GenesCCDC179, GAS2, SVIP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699208
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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