A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431653



Internal ID21089206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:67402266..67411333hg38UCSC Ensembl
chr8:68314501..68323568hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg389068
hg199068
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170536
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431653
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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