A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5612912



Internal ID21561217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:54895455..54895455hg38UCSC Ensembl
chr4:55761621..55761621hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17122338
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5612912
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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