A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000351



Internal ID21909694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56076094..56087478hg38UCSC Ensembl
chr5:55371921..55383305hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3811385
hg1911385
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17552749
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000351
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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