A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674166



Internal ID9940271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:24080836..24086044hg38UCSC Ensembl
chr7:24120455..24125663hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg385209
hg195209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6002448, essv6400762
SamplesNA11829, NA19779
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674166
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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