A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477898



Internal ID21135451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:132427433..132485561hg38UCSC Ensembl
chr12:133004019..133062147hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3858129
hg1958129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17999316
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477898
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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