A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014977



Internal ID21924320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:158422231..158423606hg38UCSC Ensembl
chr5:157849239..157850614hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg381376
hg191376
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559095
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014977
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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