A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669667



Internal ID9935772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109066863..109076603hg38UCSC Ensembl
Outerchr1:109066826..109076653hg38UCSC Ensembl
Innerchr1:109609485..109619225hg19UCSC Ensembl
Outerchr1:109609448..109619275hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg389828
hg199828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6263577
SamplesNA20785
Known GenesTAF13
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669667
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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