A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591631



Internal ID16379040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:128680780..128688780hg38UCSC Ensembl
Innerchr3:128399623..128407623hg19UCSC Ensembl
Innerchr3:129882313..129890313hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg388001
hg198001
hg188001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv973044
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591631
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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