A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873987



Internal ID22648937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3735935..3738747hg38UCSC Ensembl
chrX:3653976..3656788hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg382813
hg192813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460748
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873987
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