A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085366



Internal ID21994599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:2280405..2280405hg38UCSC Ensembl
chr12:2389571..2389571hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598362
Samples
Known GenesCACNA1C, CACNA1C-IT3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085366
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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