A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466409



Internal ID21123962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93502064..93502623hg38UCSC Ensembl
chr12:93895840..93896399hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005823
Samples
Known GenesMRPL42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466409
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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