A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413486



Internal ID21071039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:23101404..23103924hg38UCSC Ensembl
chr6:23101632..23104152hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382521
hg192521
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225677
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413486
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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