A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461483



Internal ID21119036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:106442672..106442774hg38UCSC Ensembl
chr12:106836450..106836552hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996117
Samples
Known GenesPOLR3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461483
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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