A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427539



Internal ID21085092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:107597539..107606469hg38UCSC Ensembl
chr8:108609767..108618697hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg388931
hg198931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162135
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427539
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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