A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858596



Internal ID22633531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102573148..102581040hg38UCSC Ensembl
chr14:103039485..103047377hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg387893
hg197893
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460867
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858596
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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