A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931108



Internal ID22706387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110245304..110253983hg38UCSC Ensembl
chr12:110683109..110691788hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38n/a
hg19n/a
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361438
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931108
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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