A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942432



Internal ID22717869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:105838895..105840893hg38UCSC Ensembl
chr12:106232673..106234671hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg381999
hg191999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356826
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5942432
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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