A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106522



Internal ID22015755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:73974298..73976814hg38UCSC Ensembl
chrX:73194133..73196649hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg382517
hg192517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649143
Samples
Known GenesJPX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106522
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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