A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578757



Internal ID16366166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:18280361..18282126hg38UCSC Ensembl
Innerchr19:18391171..18392936hg19UCSC Ensembl
Innerchr19:18252171..18253936hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381766
hg191766
hg181766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6296n54
Supporting Variantsnssv895778
Samples
Known GenesJUND, MIR3188
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578757
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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