A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590107



Internal ID16030830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:39315814..39356217hg38UCSC Ensembl
Innerchr3:39357305..39397708hg19UCSC Ensembl
Innerchr3:39332309..39372712hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3840404
hg1940404
hg1840404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152247
SamplesHGDP00458
Known GenesCCR8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590107
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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