A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590195



Internal ID16377604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:46756350..46779343hg38UCSC Ensembl
Innerchr3:46797840..46820833hg19UCSC Ensembl
Innerchr3:46772844..46795837hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3822994
hg1922994
hg1822994
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8305n54
Supporting Variantsnssv962573
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590195
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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