A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5987455



Internal ID21896798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:214568128..214656925hg38UCSC Ensembl
chr2:215432852..215521649hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3888798
hg1988798
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519873
Samples
Known GenesVWC2L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5987455
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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