A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666258



Internal ID9932363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:88860919..89267999hg38UCSC Ensembl
chr2:89160431..89567756hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38407081
hg19407326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv714e199
Supporting Variantsessv6005227, essv5632855
SamplesNA18940, HG00148
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666258
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