A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590814



Internal ID16378223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:84045667..84595035hg38UCSC Ensembl
Innerchr3:84094818..84644186hg19UCSC Ensembl
Innerchr3:84177508..84726876hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38549369
hg19549369
hg18549369
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv967076
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590814
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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