A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv745967



Internal ID16039923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:31146224..31155768hg38UCSC Ensembl
Innerchr10:31435153..31444697hg19UCSC Ensembl
Innerchr10:31475159..31484703hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg389545
hg199545
hg189545
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550361
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv745967
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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