A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398431



Internal ID21055984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:20214382..20216977hg38UCSC Ensembl
chr6:20214613..20217208hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382596
hg192596
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227662
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398431
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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