A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589883



Internal ID6977213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:14345099..14481144hg38UCSC Ensembl
chr2:14485223..14621268hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38136046
hg19136046
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv678e214
Supporting Variantsessv10414784, essv10414783
SamplesHG03790, NA20790
Known GenesLINC00276
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589883
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