A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467113



Internal ID21124666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:17006401..17011100hg38UCSC Ensembl
chr12:17159335..17164034hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187215
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467113
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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