A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935646



Internal ID22710991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111909158..111909215hg38UCSC Ensembl
chr12:112346962..112347019hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355760
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935646
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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