A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580157



Internal ID16367566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54220589..54233134hg38UCSC Ensembl
Innerchr19:54724411..54737010hg19UCSC Ensembl
Innerchr19:59416223..59428822hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3812546
hg1912600
hg1812600
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6547n54
Supporting Variantsnssv901409
Samples
Known GenesLILRB3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580157
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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