A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742614



Internal ID166280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:138625463..138625537hg38UCSC Ensembl
chrX:137707624..137707698hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433636
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742614
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.004215


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