A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17642236



Internal ID21834283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:121553844..121614695hg38UCSC Ensembl
chrX:120687698..120748549hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3860852
hg1960852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6100946
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17642236
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