A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166237



Internal ID21488930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:145494002..145494002hg38UCSC Ensembl
chrX:144575520..144575520hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38830
hg19830
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610555
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166237
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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