A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410053



Internal ID21067606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73511775..73517416hg38UCSC Ensembl
chr6:74221498..74227139hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg385642
hg195642
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228243
Samples
Known GenesEEF1A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410053
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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