A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417580



Internal ID21075133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89796517..89796958hg38UCSC Ensembl
chr8:90808745..90809186hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38442
hg19442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173076
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417580
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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