A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406580



Internal ID21064133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:66500701..66506200hg38UCSC Ensembl
chr5:65796529..65802028hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214846
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406580
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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