A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741557



Internal ID165223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:95138542..96064542hg38UCSC Ensembl
chrX:94393541..95319541hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38926001
hg19926001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138657
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741557
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000628009


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