A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348909



Internal ID21006462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:199183363..199196857hg38UCSC Ensembl
chr2:200048086..200061580hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3813495
hg1913495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083914
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348909
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