A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741733



Internal ID165399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101597892..101602065hg38UCSC Ensembl
chrX:100852870..100857049hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg384174
hg194180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422352
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741733
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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