A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431696



Internal ID21089249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:112954801..112963200hg38UCSC Ensembl
chr8:113967030..113975429hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg388400
hg198400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7463n223
Supporting Variantsnssv18234601
Samples
Known GenesCSMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431696
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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