A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408900



Internal ID21066453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:79135293..79146227hg38UCSC Ensembl
chr6:79845010..79855944hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3810935
hg1910935
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235045
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408900
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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