A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584711



Internal ID21533254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61518408..61521814hg38UCSC Ensembl
chr18:59185641..59189047hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg383407
hg193407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101722
SamplesHG02011
Known GenesCDH20
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584711
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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