A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465149



Internal ID21122702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:55404985..55664522hg38UCSC Ensembl
chr12:55798769..56058306hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg38259538
hg19259538
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182844
Samples
Known GenesOR10P1, OR2AP1, OR6C2, OR6C4, OR6C68, OR6C70, OR6C76
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465149
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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