A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599926



Internal ID6986971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:23532255..23575216hg38UCSC Ensembl
Innerchr4:23532255..23575216hg38UCSC Ensembl
Outerchr4:23531755..23575716hg38UCSC Ensembl
chr4:23533878..23576839hg19UCSC Ensembl
Innerchr4:23533878..23576839hg19UCSC Ensembl
Outerchr4:23533378..23577339hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3842962
hg1942962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11370538
SamplesNA20778
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599926
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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