A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579842



Internal ID16020565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43290434..43362671hg38UCSC Ensembl
Innerchr19:43794586..43866823hg19UCSC Ensembl
Innerchr19:48486426..48558663hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3872238
hg1972238
hg1872238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6502n54
Supporting Variantsnssv899894
Samples
Known GenesCD177, PRG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579842
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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