A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874212



Internal ID22649163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2358535..2371236hg38UCSC Ensembl
chrX:2276576..2289277hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3812702
hg1912702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460065
Samples
Known GenesDHRSX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874212
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