A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428509



Internal ID21086062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:59207988..59208594hg38UCSC Ensembl
chr8:60120547..60121153hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170027
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428509
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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