A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645972



Internal ID21838019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103868022..103868151hg38UCSC Ensembl
chrX:103122922..103123051hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6112438
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645972
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