A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465757



Internal ID21123310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:69704216..69706302hg38UCSC Ensembl
chr12:70097996..70100082hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg382087
hg192087
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184377
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465757
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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