A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6399425



Internal ID21056978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:78467824..78497292hg38UCSC Ensembl
chr6:79177541..79207009hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3829469
hg1929469
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230488
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6399425
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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