A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416433



Internal ID21073986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:112953801..112961200hg38UCSC Ensembl
chr8:113966030..113973429hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg387400
hg197400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7463n223
Supporting Variantsnssv18228066
Samples
Known GenesCSMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416433
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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