A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666294



Internal ID15402946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:9254351..9307196hg38UCSC Ensembl
Innerchr11:9275898..9328743hg19UCSC Ensembl
Innerchr11:9232474..9285319hg18UCSC Ensembl
Innerchr11:9232474..9285319hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3852846
hg1952846
hg1852846
hg1752846
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515891
Supporting Variants
Samples
Known GenesDENND5A, TMEM41B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666294
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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