A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424734



Internal ID21082287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21028618..21028910hg38UCSC Ensembl
chr8:20886129..20886421hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166033
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424734
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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