A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428564



Internal ID21086117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:113163837..113347937hg38UCSC Ensembl
chr8:114176066..114360166hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38184101
hg19184101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228909
Samples
Known GenesCSMD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428564
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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