A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741189



Internal ID164855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:85635139..85641947hg38UCSC Ensembl
chrX:84890144..84896952hg19UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg386809
hg196809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422774
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741189
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00312175


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