A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638451



Internal ID21586756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96622858..96622858hg38UCSC Ensembl
chr5:95958562..95958562hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38891
hg19891
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155391
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638451
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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