A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592121



Internal ID16379530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:157719279..157875681hg38UCSC Ensembl
Innerchr3:157437068..157593470hg19UCSC Ensembl
Innerchr3:158919762..159076164hg18UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38156403
hg19156403
hg18156403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv977130
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592121
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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