A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936392



Internal ID22711745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:55898186..55900527hg38UCSC Ensembl
chr12:56291970..56294311hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg382342
hg192342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365757
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936392
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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