A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671697



Internal ID9591116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:210367743..210374030hg38UCSC Ensembl
chr2:211232467..211238754hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg386288
hg196288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5787987
SamplesHG01440
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671697
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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