A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589884



Internal ID6977214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:14381792..14426970hg38UCSC Ensembl
Innerchr2:14381841..14426922hg38UCSC Ensembl
Outerchr2:14381744..14427019hg38UCSC Ensembl
chr2:14521916..14567094hg19UCSC Ensembl
Innerchr2:14521965..14567046hg19UCSC Ensembl
Outerchr2:14521868..14567143hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3845179
hg1945179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10414785, essv10414786
SamplesHG03790, NA20790
Known GenesLINC00276
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589884
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