A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486561



Internal ID21144114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:109106843..109108584hg38UCSC Ensembl
chr12:109544648..109546389hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg381742
hg191742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996247
Samples
Known GenesUNG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486561
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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