A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579668



Internal ID16367077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42802004..43234188hg38UCSC Ensembl
Innerchr19:43306156..43738340hg19UCSC Ensembl
Innerchr19:47997996..48430180hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38432185
hg19432185
hg18432185
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6467n54
Supporting Variantsnssv899667, nssv899666
Samples
Known GenesLOC100289650, LOC284344, PSG1, PSG10P, PSG11, PSG2, PSG4, PSG5, PSG6, PSG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579668
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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