A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000276



Internal ID21909619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7262340..7268946hg38UCSC Ensembl
chr5:7262453..7269059hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg386607
hg196607
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550811
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000276
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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