A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv895736



Internal ID16189692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:18280260..18281663hg38UCSC Ensembl
Innerchr19:18391070..18392473hg19UCSC Ensembl
Innerchr19:18252070..18253473hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381404
hg191404
hg181404
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578745
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)nssv895736
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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