A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5617451



Internal ID21565756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:10866..10866hg38UCSC Ensembl
chr4:10866..10866hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128065, nssv17130568
SamplesHG00732, HG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5617451
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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