A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549786



Internal ID15990509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1251048..1862404hg38UCSC Ensembl
Innerchr10:1293100..1904598hg19UCSC Ensembl
Innerchr10:1283100..1894598hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38611357
hg19611499
hg18611499
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv925n54
Supporting Variantsnssv740215
Samples
Known GenesADARB2, ADARB2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549786
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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