A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631636



Internal ID21579941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150978304..150978304hg38UCSC Ensembl
chr5:150357866..150357866hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133789
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631636
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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