A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657875



Internal ID9923980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6081635..6105441hg38UCSC Ensembl
Outerchr7:6081264..6105811hg38UCSC Ensembl
Innerchr7:6121266..6145072hg19UCSC Ensembl
Outerchr7:6120895..6145442hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3824548
hg1924548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1183e199
Supporting Variantsessv5594304, essv5770145, essv5952231, essv6067052, essv6596954, essv5493105, essv5845270, essv6039307, essv5928265, essv5702549, essv6240588, essv6378322, essv5859411, essv5869002, essv6098482, essv6257023, essv5512782, essv5936870, essv6560631, essv5814723
SamplesNA19204, NA18486, NA18504, NA19190, NA18510, NA19107, NA18916, NA19197, NA19235, NA18520, NA18867, NA18934, NA18516, NA18499, NA18856, NA18853, NA19257, NA19108, NA19248, NA19129
Known GenesUSP42
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657875
Frequency
Sample Size1151
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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