A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5874503



Internal ID8851906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26599889..26600221hg38UCSC Ensembl
chr2:26822757..26823089hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2663963
Supporting Variants
SamplesHG01125
Known GenesCIB4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5874503
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