A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15937334



Internal ID1073033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76201390..76210700hg38UCSC Ensembl
Innerchr18:76201451..76210640hg38UCSC Ensembl
Outerchr18:76201330..76210761hg38UCSC Ensembl
chr18:73913345..73922655hg19UCSC Ensembl
Innerchr18:73913406..73922595hg19UCSC Ensembl
Outerchr18:73913285..73922716hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg389311
hg199311
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643162
Supporting Variants
SamplesHG00698
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15937334
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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