A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579666



Internal ID16367075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42802004..43089269hg38UCSC Ensembl
Innerchr19:43306156..43593421hg19UCSC Ensembl
Innerchr19:47997996..48285261hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38287266
hg19287266
hg18287266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6465n54
Supporting Variantsnssv899664, nssv899663
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG2, PSG6, PSG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579666
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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