A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396258



Internal ID21053811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1275432..1329575hg38UCSC Ensembl
chr6:1275667..1329810hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3854144
hg1954144
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215524
Samples
Known GenesFOXQ1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396258
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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