A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642739



Internal ID6682819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61916660..61918424hg38UCSC Ensembl
Innerchr18:61916677..61918408hg38UCSC Ensembl
Outerchr18:61916644..61918441hg38UCSC Ensembl
chr18:59583893..59585657hg19UCSC Ensembl
Innerchr18:59583910..59585641hg19UCSC Ensembl
Outerchr18:59583877..59585674hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg381765
hg191765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15900880, essv15900881
SamplesNA18530, NA19063
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642739
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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