A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5596967



Internal ID8574370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63861180..63862856hg38UCSC Ensembl
chr2:64088314..64089990hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg381677
hg191677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658650
Supporting Variants
SamplesNA19240
Known GenesUGP2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5596967
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