A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642022



Internal ID7028792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26437526..26441120hg38UCSC Ensembl
Innerchr18:26437576..26441070hg38UCSC Ensembl
Outerchr18:26437476..26441170hg38UCSC Ensembl
chr18:24017490..24021084hg19UCSC Ensembl
Innerchr18:24017540..24021034hg19UCSC Ensembl
Outerchr18:24017440..24021134hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg383595
hg193595
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15824366
SamplesHG03717
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642022
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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