A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520963



Internal ID297271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:42652270..42652355hg38UCSC Ensembl
chr18:40232235..40232320hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17717702
Samples
Known GenesLINC00907
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520963
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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