A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661939



Internal ID15398591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25220804..25254329hg38UCSC Ensembl
Innerchr11:25242350..25275875hg19UCSC Ensembl
Innerchr11:25198926..25232451hg18UCSC Ensembl
Innerchr11:25198926..25232451hg17UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3833526
hg1933526
hg1833526
hg1733526
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516879
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661939
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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