A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666861



Internal ID9932966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24057529..24075323hg38UCSC Ensembl
chr7:24097148..24114942hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3817795
hg1917795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6174049, essv6129319
SamplesNA19982, NA19390
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666861
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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