A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405229



Internal ID21062782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84691244..84725457hg38UCSC Ensembl
chr6:85400962..85435175hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3834214
hg1934214
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228617
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405229
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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