A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17640499



Internal ID21832546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:108144026..108144148hg38UCSC Ensembl
chrX:107387256..107387378hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6108540
Supporting Variants
Samples
Known GenesATG4A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17640499
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