A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736951



Internal ID160617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:51510587..51539849hg38UCSC Ensembl
chrX:51253439..51282701hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3829263
hg1929263
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557976
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736951
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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