A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741737



Internal ID165403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101735022..101735368hg38UCSC Ensembl
chrX:100989995..100990341hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425382
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741737
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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