A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428443



Internal ID21085996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:59805359..59805935hg38UCSC Ensembl
chr8:60717918..60718494hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38577
hg19577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169739
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428443
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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