A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695901



Internal ID15432553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:120152797..120156040hg38UCSC Ensembl
Innerchr11:120023505..120026748hg19UCSC Ensembl
Innerchr11:119528715..119531958hg18UCSC Ensembl
Innerchr11:119528715..119531958hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg383244
hg193244
hg183244
hg173244
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518463
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695901
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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