A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5594262



Internal ID21542859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74738346..74738577hg38UCSC Ensembl
chr18:72450302..72450533hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101979
SamplesHG03486
Known GenesZNF407
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5594262
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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