A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867845



Internal ID22642780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:105918099..105918334hg38UCSC Ensembl
chrX:105162091..105162326hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448186
Samples
Known GenesNRK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867845
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