A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670921



Internal ID9937026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:123005165..123006690hg38UCSC Ensembl
chr8:124017405..124018930hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg381526
hg191526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6543331
SamplesNA19701
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670921
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