A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425531



Internal ID21083084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:58051699..58052626hg38UCSC Ensembl
chr8:58964258..58965185hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38928
hg19928
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226761
Samples
Known GenesFAM110B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425531
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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