A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410957



Internal ID21068510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1311201..1315000hg38UCSC Ensembl
chr6:1311436..1315235hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215556
Samples
Known GenesFOXQ1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410957
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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