A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881111



Internal ID22656084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14343749..14358498hg38UCSC Ensembl
chr16:14437606..14452355hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3814750
hg1914750
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17476260
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881111
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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