A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456846



Internal ID21114399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:97438301..97440000hg38UCSC Ensembl
chr12:97832079..97833778hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196124
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456846
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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