A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368999



Internal ID21026552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106399443..106401235hg38UCSC Ensembl
chr3:106118290..106120082hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg381793
hg191793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093747
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368999
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