A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549884



Internal ID16337293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4989168..5023056hg38UCSC Ensembl
Innerchr10:5031360..5065248hg19UCSC Ensembl
Innerchr10:5021360..5055248hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3833889
hg1933889
hg1833889
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv743473
Samples
Known GenesAKR1C2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549884
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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