A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415809



Internal ID21073362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81679344..81700704hg38UCSC Ensembl
chr8:82591579..82612939hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3821361
hg1921361
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227111
Samples
Known GenesIMPA1, SLC10A5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415809
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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