A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486635



Internal ID21144188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:123119507..123126042hg38UCSC Ensembl
chr12:123604054..123610589hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg386536
hg196536
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182296
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486635
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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