A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430921



Internal ID21088474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66189699..66193798hg38UCSC Ensembl
chr8:67101934..67106033hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226741
Samples
Known GenesLINC00967
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430921
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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