A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927186



Internal ID22702414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40872746..40975076hg38UCSC Ensembl
chr9:66825774..69048305hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38102331
hg192222532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435841
Samples
Known GenesANKRD20A1, ANKRD20A3, AQP7P1, FAM27B, FAM27E3, LOC100132352, LOC286297, LOC642236
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927186
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