A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672684



Internal ID9938789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34508073..34509319hg38UCSC Ensembl
chr18:32088037..32089283hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg381247
hg191247
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6438100
SamplesNA11993
Known GenesDTNA
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672684
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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