A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402360



Internal ID21059913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34670036..34674151hg38UCSC Ensembl
chr6:34637813..34641928hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg384116
hg194116
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235833
Samples
Known GenesC6orf106
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402360
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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