A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424545



Internal ID21082098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39852493..39861452hg38UCSC Ensembl
chr8:39710012..39718971hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg388960
hg198960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169699
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424545
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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