A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741470



Internal ID165136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:92839705..92840401hg38UCSC Ensembl
chrX:92094704..92095400hg19UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg38697
hg19697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5418475
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741470
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.007687


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