A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15857765



Internal ID5859581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:45769709..45780312hg38UCSC Ensembl
Innerchr18:45769759..45780262hg38UCSC Ensembl
Outerchr18:45769592..45780429hg38UCSC Ensembl
chr18:43349674..43360277hg19UCSC Ensembl
Innerchr18:43349724..43360227hg19UCSC Ensembl
Outerchr18:43349557..43360394hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3810604
hg1910604
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3642413
Supporting Variants
SamplesHG01882
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15857765
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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