A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367043



Internal ID21024596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122316864..122321830hg38UCSC Ensembl
chr3:122035711..122040677hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg384967
hg194967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095200
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367043
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