A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638255



Internal ID21830302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:113931159..113931222hg38UCSC Ensembl
chrX:113174435..113174506hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3864
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103906
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638255
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