A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740848



Internal ID164514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:76576650..76580112hg38UCSC Ensembl
chrX:75797042..75800504hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg383463
hg193463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5421345
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740848
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002654


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