A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655279



Internal ID21603584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74218360..74218360hg38UCSC Ensembl
chr18:71885595..71885595hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17102464
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655279
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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