A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578537



Internal ID16365946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8167850..8179517hg38UCSC Ensembl
Innerchr19:8232734..8244401hg19UCSC Ensembl
Innerchr19:8138734..8150401hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3811668
hg1911668
hg1811668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv893302
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578537
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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