A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740882



Internal ID164548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:77625637..77626026hg38UCSC Ensembl
chrX:76881105..76881494hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425635
Supporting Variants
Samples
Known GenesATRX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740882
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001874


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