A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742149



Internal ID165815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115721550..115738000hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3816451
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5429789
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742149
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.499615


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