A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5603292



Internal ID21551955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:54611370..54611608hg38UCSC Ensembl
chr18:52278601..52278839hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101820
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5603292
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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