A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642141



Internal ID6682222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31887128..31888134hg38UCSC Ensembl
Innerchr18:31887149..31888114hg38UCSC Ensembl
Outerchr18:31887108..31888155hg38UCSC Ensembl
chr18:29467091..29468097hg19UCSC Ensembl
Innerchr18:29467112..29468077hg19UCSC Ensembl
Outerchr18:29467071..29468118hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg381007
hg191007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15837720
SamplesHG02322
Known GenesTRAPPC8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642141
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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