A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv895581



Internal ID16189537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15928110..15930313hg38UCSC Ensembl
Innerchr19:16038920..16041123hg19UCSC Ensembl
Innerchr19:15899920..15902123hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382204
hg192204
hg182204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578731
Supporting Variants
Samples
Known GenesCYP4F11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv895581
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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