A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549883



Internal ID15990606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4983904..5233799hg38UCSC Ensembl
Innerchr10:5026096..5275762hg19UCSC Ensembl
Innerchr10:5016096..5265762hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38249896
hg19249667
hg18249667
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv743472
Samples
Known GenesAKR1C2, AKR1C3, AKR1C4, AKR1CL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549883
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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