A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17637979



Internal ID21830026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:97194891..97194891hg38UCSC Ensembl
chrX:96449890..96449890hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6047211
Supporting Variants
Samples
Known GenesDIAPH2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17637979
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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