A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414392



Internal ID21071945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21562212..21570404hg38UCSC Ensembl
chr6:21562443..21570635hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg388193
hg198193
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234920
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414392
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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