A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465716



Internal ID21123269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32420529..32453821hg38UCSC Ensembl
chr12:32573463..32606755hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3833293
hg1933293
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185368
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465716
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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