A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667844



Internal ID9933949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195465202..195466678hg38UCSC Ensembl
Outerchr3:195465165..195466728hg38UCSC Ensembl
Innerchr3:195185920..195187397hg19UCSC Ensembl
Outerchr3:195185883..195187447hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381564
hg191565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6395628
SamplesNA19725
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667844
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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