A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16091434



Internal ID6402477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54224126..54243061hg38UCSC Ensembl
chr19:54727998..54746910hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3818936
hg1918913
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644786
Supporting Variants
SamplesNA20351
Known GenesLILRA6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16091434
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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