A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398362



Internal ID21055915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22820922..22858881hg38UCSC Ensembl
chr6:22821151..22859110hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3837960
hg1937960
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232611
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398362
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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