A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422133



Internal ID21079686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:75309755..75331823hg38UCSC Ensembl
chr8:76221990..76244058hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3822069
hg1922069
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170178
Samples
Known GenesCASC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422133
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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