A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430121



Internal ID21087674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:75245073..75245643hg38UCSC Ensembl
chr8:76157308..76157878hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38571
hg19571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170175
Samples
Known GenesCASC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430121
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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