A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695974



Internal ID15432626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:15667845..15754728hg38UCSC Ensembl
Innerchr11:15689391..15776274hg19UCSC Ensembl
Innerchr11:15645967..15732850hg18UCSC Ensembl
Innerchr11:15645967..15732850hg17UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3886884
hg1986884
hg1886884
hg1786884
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518531
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695974
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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