A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589812



Internal ID6977142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11106221..11107309hg38UCSC Ensembl
Innerchr2:11106221..11107309hg38UCSC Ensembl
Outerchr2:11106018..11107410hg38UCSC Ensembl
chr2:11246347..11247435hg19UCSC Ensembl
Innerchr2:11246347..11247435hg19UCSC Ensembl
Outerchr2:11246144..11247536hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg381089
hg191089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10407024, essv10407025
SamplesNA19391, NA19334
Known GenesFLJ33534
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589812
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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