A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863897



Internal ID22638832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:86070526..86093095hg38UCSC Ensembl
chr14:86536870..86559439hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3822570
hg1922570
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17470320, nssv17469688
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863897
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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