A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470430



Internal ID21127983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:59950233..60071379hg38UCSC Ensembl
chr12:60344014..60465160hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38121147
hg19121147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002246
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470430
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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