A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579698



Internal ID16367107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42851743..43182176hg38UCSC Ensembl
Innerchr19:43355895..43686328hg19UCSC Ensembl
Innerchr19:48047735..48378168hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38330434
hg19330434
hg18330434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6467n54
Supporting Variantsnssv899708, nssv899707
Samples
Known GenesPSG1, PSG10P, 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)nsv579698
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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