A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580169



Internal ID16367578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54225208..54237487hg38UCSC Ensembl
Innerchr19:54729079..54741363hg19UCSC Ensembl
Innerchr19:59420891..59433175hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3812280
hg1912285
hg1812285
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6551n54
Supporting Variantsnssv901436
Samples
Known GenesLILRA6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580169
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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