A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405269



Internal ID21062822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3768317..3800749hg38UCSC Ensembl
chr6:3768551..3800983hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3832433
hg1932433
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219895
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405269
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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