A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv973055



Internal ID16267011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:128708896..128713579hg38UCSC Ensembl
Innerchr3:128427739..128432422hg19UCSC Ensembl
Innerchr3:129910429..129915112hg18UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg384684
hg194684
hg184684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv591640
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv973055
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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