A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736438



Internal ID160104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:38179837..38204000hg38UCSC Ensembl
chrX:38039090..38063253hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3824164
hg1924164
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6139025
Supporting Variants
Samples
Known GenesSRPX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736438
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000627221


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