A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425684



Internal ID21083237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:3101881..6049470hg38UCSC Ensembl
chr8:2959403..5906992hg19UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg382947590
hg192947590
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218955
Samples
Known GenesCSMD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425684
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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