A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5648558



Internal ID21596863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74218369..74218369hg38UCSC Ensembl
chr18:71885604..71885604hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101957, nssv17102283
SamplesHG03065, HG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5648558
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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