A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659191



Internal ID9925296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109941520..109943163hg38UCSC Ensembl
Outerchr1:109941477..109943213hg38UCSC Ensembl
Innerchr1:110484142..110485785hg19UCSC Ensembl
Outerchr1:110484099..110485835hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg381737
hg191737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5845724, essv6212933
SamplesHG00736, HG01047
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659191
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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