A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416943



Internal ID21074496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132890684..132891312hg38UCSC Ensembl
chr8:133902929..133903557hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18165723
Samples
Known GenesTG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416943
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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