A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5600174



Internal ID21548812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62581469..62581820hg38UCSC Ensembl
chr18:60248702..60249053hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101560
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5600174
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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