A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742040



Internal ID165706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:112836684..112836816hg38UCSC Ensembl
chrX:112079912..112080044hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415833
Supporting Variants
Samples
Known GenesAMOT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742040
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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