A curated catalogue of human genomic structural variation




Variant Details

Variant: esv988540



Internal ID7060487
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 gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv77e180
Supporting Variantsessv3586040
SamplesHuRef
Known GenesLILRA6
MethodSNP array
AnalysisPooled samples.
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv988540
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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