A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430466



Internal ID21088019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:53489252..53528770hg38UCSC Ensembl
chr8:54401812..54441330hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3839519
hg1939519
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226333
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430466
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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