A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549769



Internal ID15990492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1198080..1722772hg38UCSC Ensembl
Innerchr10:1244020..1764966hg19UCSC Ensembl
Innerchr10:1234020..1754966hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38524693
hg19520947
hg18520947
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv925n54
Supporting Variantsnssv740170
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)nsv549769
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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