A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656357



Internal ID21604662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11424597..11424597hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3868
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17103794, nssv17103793
SamplesHG00732, HG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656357
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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