A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597953



Internal ID6985090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140211113..140268183hg38UCSC Ensembl
chr3:139929955..139987025hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3857071
hg1957071
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11161215
SamplesHG03120
Known GenesCLSTN2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597953
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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