A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17741552



Internal ID165218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:95058137..95125325hg38UCSC Ensembl
chrX:94313136..94380324hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3867189
hg1967189
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5421237
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17741552
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00583212


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