A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739980



Internal ID20515955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3365914..3365966hg38UCSC Ensembl
chr2:3369685..3369737hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279863
Samples
Known GenesTSSC1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739980
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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