A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2371e59



Internal ID22763591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238520172..238521570hg38UCSC Ensembl
chr2:239428813..239430211hg19UCSC Ensembl
chr2:239093552..239094950hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg381399
hg191399
hg181399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3368551, esv3376227
SamplesNA19239, NA19240
Known GenesLINC01107
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2371e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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