A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875067



Internal ID22650021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:13311700..13311844hg38UCSC Ensembl
chrX:13329819..13329963hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431297
Samples
Known GenesLOC100093698
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875067
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