A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565786



Internal ID7037168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:54238010..54250220hg38UCSC Ensembl
Outerchr19:54741886..54754084hg19UCSC Ensembl
Outerchr19:59433698..59445896hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3817405
hg1917405
hg1817405
Variant TypeCNV insertion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1006598
Supporting Variants
SamplesHuRef
Known GenesLILRA6
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565786
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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