A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457608



Internal ID21115161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:41130580..41151021hg38UCSC Ensembl
chr12:41524382..41544823hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3820442
hg1920442
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188404
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457608
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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