A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402505



Internal ID21060058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93561761..93621670hg38UCSC Ensembl
chr6:94271479..94331388hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3859910
hg1959910
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219296
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402505
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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