A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420775



Internal ID21078328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92742744..92743608hg38UCSC Ensembl
chr8:93754972..93755836hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38865
hg19865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173479
Samples
Known GenesFLJ46284
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420775
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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