A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458307



Internal ID21115860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:80789124..80791759hg38UCSC Ensembl
chr12:81182903..81185538hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg382636
hg192636
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18003681
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458307
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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