A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667050



Internal ID21615357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:315819..315873hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167168
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667050
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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