A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361939



Internal ID21019492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149126726..149130599hg38UCSC Ensembl
chr3:148844513..148848386hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg383874
hg193874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096297
Samples
Known GenesHPS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361939
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