A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888894



Internal ID22663904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106580154..106580234hg38UCSC Ensembl
chr6:107028029..107028109hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17427062
Samples
Known GenesRTN4IP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888894
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer