A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670666



Internal ID9936771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:107638159..107640660hg38UCSC Ensembl
Outerchr3:107638122..107640718hg38UCSC Ensembl
Innerchr3:107357006..107359507hg19UCSC Ensembl
Outerchr3:107356969..107359565hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg382597
hg192597
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6354004
SamplesHG00245
Known GenesBBX
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670666
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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