A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420558



Internal ID21078111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:24034234..24040910hg38UCSC Ensembl
chr8:23891747..23898423hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg386677
hg196677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167168
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420558
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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