A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421578



Internal ID21079131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:58188675..58229729hg38UCSC Ensembl
chr8:59101234..59142288hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3841055
hg1941055
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169953
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421578
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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