A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580200



Internal ID16367609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54230309..54232863hg38UCSC Ensembl
Innerchr19:54734184..54736739hg19UCSC Ensembl
Innerchr19:59425996..59428551hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg382555
hg192556
hg182556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6556n54
Supporting Variantsnssv901500
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580200
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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