A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579706



Internal ID16367115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42866627..43182176hg38UCSC Ensembl
Innerchr19:43370779..43686328hg19UCSC Ensembl
Innerchr19:48062619..48378168hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38315550
hg19315550
hg18315550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6467n54
Supporting Variantsnssv899717
Samples
Known GenesPSG1, PSG11, PSG2, PSG5, PSG6, PSG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579706
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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