A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736801



Internal ID160467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47517951..47521796hg38UCSC Ensembl
chrX:47377350..47381195hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg383846
hg193846
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563958
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736801
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001561


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