A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579692



Internal ID16367101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42818147..43035037hg38UCSC Ensembl
Innerchr19:43322299..43539189hg19UCSC Ensembl
Innerchr19:48014139..48231029hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38216891
hg19216891
hg18216891
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6465n54
Supporting Variantsnssv899700
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG6, PSG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579692
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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