A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740658



Internal ID164324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:71641696..71642496hg38UCSC Ensembl
chrX:70861546..70862346hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5429458
Supporting Variants
Samples
Known GenesBCYRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740658
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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