A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737937



Internal ID161603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:150085664..150086137hg38UCSC Ensembl
chrX:149253895..149254368hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556367
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737937
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000781


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