A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428448



Internal ID21086001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:128221230..128223161hg38UCSC Ensembl
chr8:129233476..129235407hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg381932
hg191932
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18163835
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428448
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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