A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873512



Internal ID22648460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:36371621..36371825hg38UCSC Ensembl
chrX:36389736..36389940hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453280
Samples
Known GenesCXorf30
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873512
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