A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589766



Internal ID16377175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:13639952..13640658hg38UCSC Ensembl
Innerchr3:13681452..13682158hg19UCSC Ensembl
Innerchr3:13656453..13657159hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38707
hg19707
hg18707
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959435
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589766
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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