A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586040



Internal ID7057422
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv988540
Supporting Variants
SamplesHuRef
Known GenesLILRA6
MethodSNP array
AnalysisPooled samples.
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586040
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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