A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643162



Internal ID7029931
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15937334, essv15937335, essv15937336
SamplesNA06984, HG03061, HG00698
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643162
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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