A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741969



Internal ID165635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:110817000..110832542hg38UCSC Ensembl
chrX:110060228..110075770hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3815543
hg1915543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422547
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741969
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00146535


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