A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660329



Internal ID9926434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98423194..98423717hg38UCSC Ensembl
chr7:98052506..98053029hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6080875, essv5762142, essv5687582
SamplesHG00442, HG00671, NA18549
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660329
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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