A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968729



Internal ID22743664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3023917..3036349hg38UCSC Ensembl
chrX:2941958..2954390hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3812433
hg1912433
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516122
Samples
Known GenesARSH
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968729
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer