A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6490151



Internal ID21147704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110863649..110866237hg38UCSC Ensembl
chr12:111301453..111304041hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg382589
hg192589
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184761
Samples
Known GenesCCDC63
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6490151
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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