A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642025



Internal ID7028795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26750305..26761015hg38UCSC Ensembl
Innerchr18:26750455..26760865hg38UCSC Ensembl
Outerchr18:26750155..26761165hg38UCSC Ensembl
chr18:24330269..24340979hg19UCSC Ensembl
Innerchr18:24330419..24340829hg19UCSC Ensembl
Outerchr18:24330119..24341129hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3810711
hg1910711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15824372
SamplesHG00656
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642025
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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