A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5650462



Internal ID21598767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:20958934..20958934hg38UCSC Ensembl
chr18:18538895..18538895hg19UCSC Ensembl
Cytoband18q11.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17100372
SamplesHG03371
Known GenesROCK1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5650462
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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