A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428691



Internal ID21086244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:48960801..48967800hg38UCSC Ensembl
chr8:49873360..49880359hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg387000
hg197000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7332n223
Supporting Variantsnssv18235193
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428691
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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