A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923959



Internal ID22699186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25520487..25529612hg38UCSC Ensembl
chr12:25673421..25682546hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg389126
hg199126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350954
Samples
Known GenesIFLTD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923959
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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