A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460637



Internal ID21118190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:45730701..45735800hg38UCSC Ensembl
chr12:46124484..46129583hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185231
Samples
Known GenesARID2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460637
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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