A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106534



Internal ID22015767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:137323165..137332628hg38UCSC Ensembl
chrX:136405324..136414787hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg389464
hg199464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645296
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106534
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