A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400428



Internal ID21057981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:78189101..78341100hg38UCSC Ensembl
chr6:78898818..79050817hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38152000
hg19152000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6278n223
Supporting Variantsnssv18222417
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400428
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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