A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423585



Internal ID21081138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:35792852..36438718hg38UCSC Ensembl
chr8:35650370..36296236hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38645867
hg19645867
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231416
Samples
Known GenesUNC5D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423585
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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