A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370192



Internal ID21027745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122477995..122478527hg38UCSC Ensembl
chr3:122196842..122197374hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095205
Samples
Known GenesKPNA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370192
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