A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736085



Internal ID159751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2966914..2967009hg38UCSC Ensembl
chrX:2884955..2885050hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424852
Supporting Variants
Samples
Known GenesARSE
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736085
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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