A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465123



Internal ID21122676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6877039..6878782hg38UCSC Ensembl
chr12:6986203..6987946hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg381744
hg191744
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178695
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465123
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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