A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736436



Internal ID160102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:38151471..38151522hg38UCSC Ensembl
chrX:38010724..38010775hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5561869
Supporting Variants
Samples
Known GenesSRPX
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736436
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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