A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15927383



Internal ID1903011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:69482285..69484365hg38UCSC Ensembl
Innerchr18:69482291..69484359hg38UCSC Ensembl
Outerchr18:69482279..69484371hg38UCSC Ensembl
chr18:67149521..67151601hg19UCSC Ensembl
Innerchr18:67149527..67151595hg19UCSC Ensembl
Outerchr18:67149515..67151607hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg382081
hg192081
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3642966
Supporting Variants
SamplesHG01786
Known GenesDOK6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15927383
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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