A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740535



Internal ID164201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:68553653..68553779hg38UCSC Ensembl
chrX:67773495..67773621hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559429
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740535
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.028411


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