A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343811



Internal ID21001364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:208597043..208796994hg38UCSC Ensembl
chr2:209461768..209661718hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38199952
hg19199951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082672
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343811
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