A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674974



Internal ID9594393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110948807..110987520hg38UCSC Ensembl
chr10:112708565..112747278hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3838714
hg1938714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5414071
SamplesHG01353
Known GenesSHOC2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674974
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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