A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739190



Internal ID162856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9403488..9411744hg38UCSC Ensembl
chrX:9371528..9379784hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg388257
hg198257
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5428183
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739190
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.5


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