A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17740613



Internal ID164279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:70715156..70730037hg38UCSC Ensembl
chrX:69935006..69949887hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3814882
hg1914882
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5536270
Supporting Variants
Samples
Known GenesTEX11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17740613
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.084322


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