A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475050



Internal ID21132603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:39159209..39178682hg38UCSC Ensembl
chr12:39553011..39572484hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3819474
hg1919474
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194810
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475050
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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