A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580227



Internal ID16367636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54242679..54265351hg38UCSC Ensembl
Innerchr19:54746528..54769205hg19UCSC Ensembl
Innerchr19:59438340..59461017hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3822673
hg1922678
hg1822678
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv901618
Samples
Known GenesLILRA6, LILRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580227
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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