A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599830



Internal ID6986875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:20004849..20015496hg38UCSC Ensembl
chr4:20006472..20017119hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg3810648
hg1910648
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11365943, essv11365942
SamplesNA19060, HG03989
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599830
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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