A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659357



Internal ID9578776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1655646..1721855hg38UCSC Ensembl
Outerchr1:1655612..1721890hg38UCSC Ensembl
Innerchr1:1587100..1653294hg19UCSC Ensembl
Outerchr1:1587066..1653329hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3866279
hg1966264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2e199
Supporting Variantsessv5874268, essv6500381
SamplesNA12400, NA18982
Known GenesCDK11A, CDK11B, MMP23A, SLC35E2B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659357
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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