A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672073



Internal ID9938178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102529901..102531211hg38UCSC Ensembl
chr10:104289658..104290968hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg381311
hg191311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5781659, essv6389566, essv5966513, essv5463193, essv6106773
SamplesNA19058, NA18964, NA19082, NA19077, NA19085
Known GenesSUFU
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672073
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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