A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666935



Internal ID9933040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21368770..21370744hg38UCSC Ensembl
chr7:21408388..21410362hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381975
hg191975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5738896, essv5624343, essv6331621
SamplesNA19374, NA19435, NA19438
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666935
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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