A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520763



Internal ID15448056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:80302905..80348854hg38UCSC Ensembl
Innerchr10:82062661..82108610hg19UCSC Ensembl
Innerchr10:82052641..82098590hg18UCSC Ensembl
Innerchr10:82052641..82098590hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3845950
hg1945950
hg1845950
hg1745950
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697597
Samples
Known GenesDYDC1, DYDC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520763
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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