A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5672261



Internal ID21620566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154519722..154519819hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166286
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5672261
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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