A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643157



Internal ID7029926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76065114..76074433hg38UCSC Ensembl
Innerchr18:76065118..76074429hg38UCSC Ensembl
Outerchr18:76065110..76074437hg38UCSC Ensembl
chr18:73777069..73786388hg19UCSC Ensembl
Innerchr18:73777073..73786384hg19UCSC Ensembl
Outerchr18:73777065..73786392hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg389320
hg199320
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15936295, essv15936297, essv15936296, essv15936292, essv15936293, essv15936294
SamplesHG00442, HG02395, NA06984, NA18560, HG03061, HG02391
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643157
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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