A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399538



Internal ID21057091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:80802301..80853000hg38UCSC Ensembl
chr6:81512018..81562717hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3850700
hg1950700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6292n223
Supporting Variantsnssv18217722
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399538
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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