A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737193



Internal ID160859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:116691958..116694572hg38UCSC Ensembl
chrX:115825926..115828540hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg382615
hg192615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432567
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737193
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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