A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631992



Internal ID21580297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:165374412..165374412hg38UCSC Ensembl
chr5:164801418..164801418hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123374
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631992
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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