A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740545



Internal ID164211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:68630967..68688302hg38UCSC Ensembl
chrX:67850809..67908144hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3857336
hg1957336
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147267
Supporting Variants
Samples
Known GenesSTARD8
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740545
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.010775


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