A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740872



Internal ID164538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:77198141..77204904hg38UCSC Ensembl
chrX:76418604..76425367hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg386764
hg196764
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415381
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740872
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0024974


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