A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595079



Internal ID6982398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4045635..4082921hg38UCSC Ensembl
chr3:4087319..4124605hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3837287
hg1937287
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv863e214
Supporting Variantsessv10903534, essv10903532, essv10903533, essv10903535
SamplesNA19701, HG01305, NA20798, NA20903
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595079
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