A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740845



Internal ID164511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:76510542..76621600hg38UCSC Ensembl
chrX:75730955..75842009hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg38111059
hg19111055
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138291
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740845
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00292826


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