A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871521



Internal ID22646459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9229920..9277340hg38UCSC Ensembl
chr16:9323777..9371197hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3847421
hg1947421
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474834
Samples
Known GenesMIR548X
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871521
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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