A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662116



Internal ID21610421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:52497351..52497351hg38UCSC Ensembl
chr18:50023721..50023721hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101508
SamplesHG03371
Known GenesDCC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662116
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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