A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643153



Internal ID7029922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75863067..75871492hg38UCSC Ensembl
Innerchr18:75863085..75871474hg38UCSC Ensembl
Outerchr18:75863049..75871510hg38UCSC Ensembl
chr18:73575022..73583447hg19UCSC Ensembl
Innerchr18:73575040..73583429hg19UCSC Ensembl
Outerchr18:73575004..73583465hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg388426
hg198426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15935924, essv15935923
SamplesNA06984, NA18977
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643153
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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