A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456824



Internal ID21114377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93476456..93479161hg38UCSC Ensembl
chr12:93870232..93872937hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg382706
hg192706
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005820
Samples
Known GenesMRPL42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456824
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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