A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367065



Internal ID21024618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65166977..65167417hg38UCSC Ensembl
chr3:65152652..65153092hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38441
hg19441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18101558
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367065
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