A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739021



Internal ID162687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:2531036..2924507hg38UCSC Ensembl
chrX:2449077..2842548hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38393472
hg19393472
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431814
Supporting Variants
Samples
Known GenesARSD, CD99, CD99P1, GYG2, LINC00102, MIR6089-1, MIR6089-2, XG, XGPY2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739021
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00041632


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