A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419916



Internal ID21077469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:64331889..64344628hg38UCSC Ensembl
chr8:65244446..65257185hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3812740
hg1912740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168817
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419916
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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