A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344726



Internal ID21002279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:168371527..168372189hg38UCSC Ensembl
chr2:169228037..169228699hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38663
hg19663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079344
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344726
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