A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv898293



Internal ID16192249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:31238200..31271998hg38UCSC Ensembl
Innerchr19:31729106..31762904hg19UCSC Ensembl
Innerchr19:36420946..36454744hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3833799
hg1933799
hg1833799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579299
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv898293
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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