A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420395



Internal ID21077948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:36394429..36490505hg38UCSC Ensembl
chr8:36251947..36348023hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3896077
hg1996077
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235771
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420395
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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