A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429277



Internal ID21086830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:59825242..59832138hg38UCSC Ensembl
chr8:60737801..60744697hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg386897
hg196897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169742
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429277
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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