A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580114



Internal ID16020837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54050443..54056824hg38UCSC Ensembl
Innerchr19:54553697..54560078hg19UCSC Ensembl
Innerchr19:59245509..59251890hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg386382
hg196382
hg186382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6541n54
Supporting Variantsnssv901192
Samples
Known GenesVSTM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580114
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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