A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434483



Internal ID21092036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:55793876..55807186hg38UCSC Ensembl
chr8:56706435..56719745hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3813311
hg1913311
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219802
Samples
Known GenesTGS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434483
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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