A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403471



Internal ID21061024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:86644270..86749922hg38UCSC Ensembl
chr6:87353988..87459640hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38105653
hg19105653
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230403
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403471
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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