A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17164999



Internal ID21511655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102184284..102184284hg38UCSC Ensembl
chrX:101439257..101439257hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg381568
hg191568
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5618364
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17164999
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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