A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859602



Internal ID22634537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25520449..25529658hg38UCSC Ensembl
chr12:25673383..25682592hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg389210
hg199210
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456192
Samples
Known GenesIFLTD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859602
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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