A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366880



Internal ID21024433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:121775157..121777117hg38UCSC Ensembl
chr3:121494004..121495964hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg381961
hg191961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095176
Samples
Known GenesIQCB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366880
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