A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673093



Internal ID9592512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63313514..63338046hg38UCSC Ensembl
chr2:63540649..63565181hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3824533
hg1924533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5478214
SamplesHG00671
Known GenesWDPCP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673093
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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