A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17164852



Internal ID21486949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:100853337..100853337hg38UCSC Ensembl
chrX:100108326..100108326hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5608530
Supporting Variants
SamplesNA12878
Known GenesNOX1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17164852
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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