A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344757



Internal ID21002310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:139667781..139670560hg38UCSC Ensembl
chr2:140425350..140428129hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg382780
hg192780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077435
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344757
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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