A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578759



Internal ID16019482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:18636196..18637035hg38UCSC Ensembl
Innerchr19:18747006..18747845hg19UCSC Ensembl
Innerchr19:18608006..18608845hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38840
hg19840
hg18840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv895781
Samples
Known GenesKLHL26
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578759
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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