A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596429



Internal ID6636700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65924258..65950258hg38UCSC Ensembl
chr3:65909933..65935933hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3826001
hg1926001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11030370, essv11030368, essv11030369
SamplesNA19035, NA19321, HG01254
Known GenesMAGI1, MAGI1-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596429
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