A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424113



Internal ID21081666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29815010..29815447hg38UCSC Ensembl
chr8:29672526..29672963hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38438
hg19438
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226161
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424113
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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