A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549882



Internal ID15990605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4901326..5161901hg38UCSC Ensembl
Innerchr10:4943518..5203864hg19UCSC Ensembl
Innerchr10:4933518..5193864hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38260576
hg19260347
hg18260347
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv743471
Samples
Known GenesAKR1C1, AKR1C2, AKR1C3, AKR1C6P, AKR1CL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549882
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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