A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373685



Internal ID21031238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:28840613..28841716hg38UCSC Ensembl
chr3:28882104..28883207hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg381104
hg191104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101381
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373685
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