A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580026



Internal ID16020749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52433847..52556619hg38UCSC Ensembl
Innerchr19:52937100..53059872hg19UCSC Ensembl
Innerchr19:57628912..57751684hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38122773
hg19122773
hg18122773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv901084
Samples
Known GenesZNF534, ZNF578, ZNF808
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580026
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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