A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741707



Internal ID165373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101098974..101098980hg38UCSC Ensembl
chrX:100353963..100353969hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg387
hg197
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554483
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741707
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001717


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