A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549794



Internal ID15990517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1558140..1558888hg38UCSC Ensembl
Innerchr10:1600335..1601083hg19UCSC Ensembl
Innerchr10:1590335..1591083hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38749
hg19749
hg18749
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv931n54
Supporting Variantsnssv740226, nssv740225
Samples
Known GenesADARB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549794
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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