A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419421



Internal ID21076974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:57360079..57437407hg38UCSC Ensembl
chr8:58272638..58349966hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3877329
hg1977329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169880
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419421
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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