A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435036



Internal ID21092589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:113358001..113403600hg38UCSC Ensembl
chr8:114370230..114415829hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3845600
hg1945600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222293
Samples
Known GenesCSMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435036
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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