A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419183



Internal ID21076736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:77649622..77658873hg38UCSC Ensembl
chr8:78561858..78571109hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg389252
hg199252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170446
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419183
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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