A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645042



Internal ID21593347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63361017..63361017hg38UCSC Ensembl
chr18:61028250..61028250hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101885, nssv17101886
SamplesHG03125, HG00731
Known GenesKDSR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645042
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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