A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631633



Internal ID21579938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:166683471..166683471hg38UCSC Ensembl
chr5:166110476..166110476hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139275
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631633
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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