A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694996



Internal ID15431648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:58345478..58347511hg38UCSC Ensembl
Innerchr11:58112951..58114984hg19UCSC Ensembl
Innerchr11:57869527..57871560hg18UCSC Ensembl
Innerchr11:57869527..57871560hg17UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg382034
hg192034
hg182034
hg172034
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522219
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694996
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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