A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740883



Internal ID164549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:77625975..77626194hg38UCSC Ensembl
chrX:76881443..76881680hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38220
hg19238
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5429938
Supporting Variants
Samples
Known GenesATRX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740883
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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