A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579843



Internal ID16020566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43290434..43366735hg38UCSC Ensembl
Innerchr19:43794586..43870887hg19UCSC Ensembl
Innerchr19:48486426..48562727hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3876302
hg1976302
hg1876302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6502n54
Supporting Variantsnssv899895
Samples
Known GenesCD177, PRG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579843
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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