A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736552



Internal ID160218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:41203967..41203974hg38UCSC Ensembl
chrX:41063220..41063227hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5543403
Supporting Variants
Samples
Known GenesUSP9X
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736552
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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