A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590076



Internal ID16377485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37936223..37951049hg38UCSC Ensembl
Innerchr3:37977714..37992540hg19UCSC Ensembl
Innerchr3:37952718..37967544hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3814827
hg1914827
hg1814827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv962177, nssv962176
Samples
Known GenesCTDSPL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590076
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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