A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549881



Internal ID15990604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4859606..5277716hg38UCSC Ensembl
Innerchr10:4901798..5319679hg19UCSC Ensembl
Innerchr10:4891798..5309679hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38418111
hg19417882
hg18417882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv743470
Samples
Known GenesAKR1C1, AKR1C2, AKR1C3, AKR1C4, AKR1C6P, AKR1CL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549881
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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