A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656704



Internal ID9922809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:27255733..27257648hg38UCSC Ensembl
chr7:27295352..27297267hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg381916
hg191916
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6511949, essv5991725, essv6554776, essv6263261, essv6425433, essv6165369, essv5645188, essv5659918, essv6213825, essv5826119, essv5671953
SamplesNA19466, NA19904, NA19384, NA19383, NA19235, NA19247, NA18516, NA18499, NA19375, NA19473, NA19472
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656704
Frequency
Sample Size1151
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer