A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352978



Internal ID21010531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:199659201..199659500hg38UCSC Ensembl
chr2:200523924..200524223hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083949
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352978
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