A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578732



Internal ID16366141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15928643..15930962hg38UCSC Ensembl
Innerchr19:16039453..16041772hg19UCSC Ensembl
Innerchr19:15900453..15902772hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg382320
hg192320
hg182320
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6291n54
Supporting Variantsnssv895582
Samples
Known GenesCYP4F11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578732
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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