A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578750



Internal ID16366159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:18280260..18282302hg38UCSC Ensembl
Innerchr19:18391070..18393112hg19UCSC Ensembl
Innerchr19:18252070..18254112hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg382043
hg192043
hg182043
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6295n54
Supporting Variantsnssv895767
Samples
Known GenesJUND, MIR3188
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578750
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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