A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv897035



Internal ID16190991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27245155..27681759hg38UCSC Ensembl
Innerchr19:27736063..28172667hg19UCSC Ensembl
Innerchr19:32427903..32864507hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38436605
hg19436605
hg18436605
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579125
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)nssv897035
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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