A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641805



Internal ID7028576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11665650..11666106hg38UCSC Ensembl
Innerchr18:11665657..11666099hg38UCSC Ensembl
Outerchr18:11665643..11666113hg38UCSC Ensembl
chr18:11665649..11666105hg19UCSC Ensembl
Innerchr18:11665656..11666098hg19UCSC Ensembl
Outerchr18:11665642..11666112hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38457
hg19457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15807331, essv15807330, essv15807332, essv15807329, essv15807333
SamplesNA19028, NA20321, NA19448, HG03079, NA19035
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641805
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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