A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472233



Internal ID21129786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93304041..93333053hg38UCSC Ensembl
chr12:93697817..93726829hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3829013
hg1929013
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005810
Samples
Known GenesLOC643339
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472233
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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