A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879505



Internal ID22654474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:17619311..17620042hg38UCSC Ensembl
chrX:17637431..17638162hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg38732
hg19732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17443034
Samples
Known GenesNHS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879505
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