A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550149



Internal ID16337558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20476185..20520884hg38UCSC Ensembl
Innerchr10:20765114..20809813hg19UCSC Ensembl
Innerchr10:20805120..20849819hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3844700
hg1944700
hg1844700
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv744322
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550149
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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