A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv895585



Internal ID15842855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:16897033..16898561hg38UCSC Ensembl
Innerchr19:17007844..17009372hg19UCSC Ensembl
Innerchr19:16868844..16870372hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381529
hg191529
hg181529
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578736
Supporting Variants
Samples
Known GenesCPAMD8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv895585
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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