A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579400



Internal ID16020123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35269128..35269961hg38UCSC Ensembl
Innerchr19:35760031..35760864hg19UCSC Ensembl
Innerchr19:40451871..40452704hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38834
hg19834
hg18834
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv898782, nssv898783
Samples
Known GenesUSF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579400
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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