A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876063



Internal ID22651023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154459875..154459946hg38UCSC Ensembl
chrX:153688215..153688286hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448703
Samples
Known GenesPLXNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876063
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