A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736863



Internal ID160529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:48607458..48607573hg38UCSC Ensembl
chrX:48465846..48465961hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5538104
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736863
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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