A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597263



Internal ID6972197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:104733180..104756606hg38UCSC Ensembl
chr3:104452024..104475450hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3823427
hg1923427
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11093179
SamplesNA18966
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597263
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