A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600619



Internal ID6987661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:58055433..58068261hg38UCSC Ensembl
Innerchr4:58055483..58068211hg38UCSC Ensembl
Outerchr4:58055355..58068339hg38UCSC Ensembl
chr4:58921599..58934427hg19UCSC Ensembl
Innerchr4:58921649..58934377hg19UCSC Ensembl
Outerchr4:58921521..58934505hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3812829
hg1912829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11444823, essv11444822, essv11444821
SamplesNA20539, NA20518, HG02102
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600619
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