A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589730



Internal ID6977059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:6747557..6757391hg38UCSC Ensembl
chr2:6887688..6897522hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg389835
hg199835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10403798, essv10403797, essv10403796
SamplesNA19466, NA19471, HG02982
Known GenesLINC00487
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589730
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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