A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589850



Internal ID6977180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:13641435..13642789hg38UCSC Ensembl
Innerchr2:13641481..13642744hg38UCSC Ensembl
Outerchr2:13641390..13642835hg38UCSC Ensembl
chr2:13781560..13782914hg19UCSC Ensembl
Innerchr2:13781606..13782869hg19UCSC Ensembl
Outerchr2:13781515..13782960hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg381355
hg191355
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10412842, essv10412843, essv10412845, essv10412844
SamplesHG02922, HG01176, HG03120, HG02923
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589850
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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