A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741939



Internal ID165605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:109854918..109866612hg38UCSC Ensembl
chrX:109098147..109109841hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3811695
hg1911695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5428593
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741939
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00187305


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