A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740738



Internal ID164404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:73813707..73813851hg38UCSC Ensembl
chrX:73033542..73033686hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416387
Supporting Variants
Samples
Known GenesTSIX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740738
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003434


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