A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578717



Internal ID16019440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15159994..15241561hg38UCSC Ensembl
Innerchr19:15270805..15352372hg19UCSC Ensembl
Innerchr19:15131805..15213372hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3881568
hg1981568
hg1881568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv895573
Samples
Known GenesBRD4, EPHX3, MIR6795, NOTCH3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578717
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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