A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167594



Internal ID21492556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47090909..47090909hg38UCSC Ensembl
chrX:46950308..46950308hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5611618
Supporting Variants
SamplesNA19238
Known GenesRGN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167594
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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