A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580201



Internal ID16367610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54230309..54233042hg38UCSC Ensembl
Innerchr19:54734184..54736918hg19UCSC Ensembl
Innerchr19:59425996..59428730hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg382734
hg192735
hg182735
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6556n54
Supporting Variantsnssv901501
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580201
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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