A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737191



Internal ID160857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:116654136..116713058hg38UCSC Ensembl
chrX:115788104..115847026hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3858923
hg1958923
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5414875
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737191
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0037461


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