A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590052



Internal ID16377461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:34868680..34896055hg38UCSC Ensembl
Innerchr3:34910172..34937547hg19UCSC Ensembl
Innerchr3:34885176..34912551hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3827376
hg1927376
hg1827376
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv962130
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590052
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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