A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875206



Internal ID22650163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24972218..24975269hg38UCSC Ensembl
chrX:24990335..24993386hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg383052
hg193052
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453916
Samples
Known GenesPOLA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875206
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