A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431111



Internal ID21088664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:48072945..48145977hg38UCSC Ensembl
chr8:48985505..49058537hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3873033
hg1973033
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233517
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431111
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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