A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413483



Internal ID21071036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73284242..73288701hg38UCSC Ensembl
chr6:73993965..73998424hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg384460
hg194460
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220460
Samples
Known GenesC6orf147, KHDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413483
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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