A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6348590



Internal ID21006143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:98760378..98763612hg38UCSC Ensembl
chr2:99376841..99380075hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg383235
hg193235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090490
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6348590
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