A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017715



Internal ID21927058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157937987..157947062hg38UCSC Ensembl
chr5:157364995..157374070hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg389076
hg199076
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574413
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017715
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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