A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590194



Internal ID16377603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46756350..46776186hg38UCSC Ensembl
Innerchr3:46797840..46817676hg19UCSC Ensembl
Innerchr3:46772844..46792680hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3819837
hg1919837
hg1819837
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8305n54
Supporting Variantsnssv962572
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590194
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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