A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv895779



Internal ID16189735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:18280521..18281941hg38UCSC Ensembl
Innerchr19:18391331..18392751hg19UCSC Ensembl
Innerchr19:18252331..18253751hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381421
hg191421
hg181421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578758
Supporting Variants
Samples
Known GenesJUND
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv895779
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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