A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580272



Internal ID16020995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54755316..54761683hg38UCSC Ensembl
Innerchr19:55266768..55273135hg19UCSC Ensembl
Innerchr19:59958580..59964947hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg386368
hg196368
hg186368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv901684, nssv901683, nssv901685, nssv901686
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580272
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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