A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167534



Internal ID21410996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:63185561..63193183hg38UCSC Ensembl
chrX:62405234..62413251hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg387623
hg198018
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5664804
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167534
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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