A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677955



Internal ID9597374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74196273..74197430hg38UCSC Ensembl
chr10:75956031..75957188hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg381158
hg191158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5701773, essv5638709
SamplesNA19382, NA19381
Known GenesADK
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677955
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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