A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472224



Internal ID21129777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:60162501..60164800hg38UCSC Ensembl
chr12:60556282..60558581hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195864
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472224
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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