A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578718



Internal ID16366127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15654151..15656056hg38UCSC Ensembl
Innerchr19:15764961..15766866hg19UCSC Ensembl
Innerchr19:15625961..15627866hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg381906
hg191906
hg181906
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv895574
Samples
Known GenesCYP4F3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578718
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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