A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17164988



Internal ID21512774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101597550..101616245hg38UCSC Ensembl
chrX:100852528..100871235hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3818696
hg1918708
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670290
Supporting Variants
Samples
Known GenesARMCX6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17164988
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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