A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645272



Internal ID21837319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:18356180..18356291hg38UCSC Ensembl
chrX:18374300..18374411hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103692
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645272
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