A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677822



Internal ID2910909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:122240883..122244347hg38UCSC Ensembl
Outerchr3:122240726..122244500hg38UCSC Ensembl
Innerchr3:121959730..121963194hg19UCSC Ensembl
Outerchr3:121959573..121963347hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg383775
hg193775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5936992
SamplesNA19835
Known GenesCASR
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677822
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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