A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918869



Internal ID22694091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:18025858..18029032hg38UCSC Ensembl
chr12:18178792..18181966hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg383175
hg193175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357363
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918869
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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