A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057808



Internal ID21967041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:47834661..48511489hg38UCSC Ensembl
chr20:46463405..47131712hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38676829
hg19668308
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17625718
Samples
Known GenesLINC00494
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057808
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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