A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462427



Internal ID21119980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:41971038..41985585hg38UCSC Ensembl
chr12:42364840..42379387hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3814548
hg1914548
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196886
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462427
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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