A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410795



Internal ID21068348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:40345948..40352908hg38UCSC Ensembl
chr6:40313687..40320647hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg386961
hg196961
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220372
Samples
Known GenesLINC00951
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410795
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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