A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17736335



Internal ID160001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:28572586..28573272hg38UCSC Ensembl
chrX:28590703..28591389hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38687
hg19687
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5549071
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17736335
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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