A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404631



Internal ID21062184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69381039..69423433hg38UCSC Ensembl
chr6:70090931..70133325hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3842395
hg1942395
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228810
Samples
Known GenesBAI3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404631
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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