A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579702



Internal ID16367111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42857733..43090267hg38UCSC Ensembl
Innerchr19:43361885..43594419hg19UCSC Ensembl
Innerchr19:48053725..48286259hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38232535
hg19232535
hg18232535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899712
Samples
Known GenesPSG1, PSG11, PSG2, PSG6, PSG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579702
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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