A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739207



Internal ID162873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9824114..9832284hg38UCSC Ensembl
chrX:9792154..9800324hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg388171
hg198171
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5419324
Supporting Variants
Samples
Known GenesSHROOM2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739207
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00353945


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