A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699526



Internal ID15436178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:103173309..103185951hg38UCSC Ensembl
Innerchr11:103044038..103056680hg19UCSC Ensembl
Innerchr11:102549248..102561890hg18UCSC Ensembl
Innerchr11:102549248..102561890hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3812643
hg1912643
hg1812643
hg1712643
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523713
Supporting Variants
Samples
Known GenesDYNC2H1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699526
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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