A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489140



Internal ID21146693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:131416458..131681827hg38UCSC Ensembl
chr12:131901003..132166372hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38265370
hg19265370
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182124
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489140
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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