A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549795



Internal ID15990518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1558294..1558888hg38UCSC Ensembl
Innerchr10:1600489..1601083hg19UCSC Ensembl
Innerchr10:1590489..1591083hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38595
hg19595
hg18595
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv740229, nssv740227, nssv740228
Samples
Known GenesADARB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549795
Frequency
Sample Size17421
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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