A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740476



Internal ID164142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:67192542..67222542hg38UCSC Ensembl
chrX:66412384..66442384hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3830001
hg1930001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6139054
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740476
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000628272


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