A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579733



Internal ID16367142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42889774..43142596hg38UCSC Ensembl
Innerchr19:43393926..43646748hg19UCSC Ensembl
Innerchr19:48085766..48338588hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38252823
hg19252823
hg18252823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6474n54
Supporting Variantsnssv899771
Samples
Known GenesPSG11, PSG2, PSG6, PSG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579733
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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