A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150184



Internal ID15855400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54227805..54239341hg38UCSC Ensembl
Innerchr19:54731679..54743217hg19UCSC Ensembl
Innerchr19:59423491..59435029hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3811537
hg1911539
hg1811539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580190
Supporting Variants
Samples1780862584_A
Known GenesLILRA6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150184
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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