A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737583



Internal ID161249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:130578396..130578431hg38UCSC Ensembl
chrX:129712370..129712405hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg38369
hg19369
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554239
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737583
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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