A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742038



Internal ID165704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:112814495..112814661hg38UCSC Ensembl
chrX:112057723..112057889hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5430176
Supporting Variants
Samples
Known GenesAMOT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742038
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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