A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549961



Internal ID16337370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:9719775..9812052hg38UCSC Ensembl
Innerchr10:9761738..9854015hg19UCSC Ensembl
Innerchr10:9801744..9894021hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3892278
hg1992278
hg1892278
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744003
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549961
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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