A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411402



Internal ID21068955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:68613298..68635771hg38UCSC Ensembl
chr6:69323190..69345663hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3822474
hg1922474
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234028
Samples
Known GenesBAI3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411402
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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