A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873088



Internal ID22648031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57878579..57880975hg38UCSC Ensembl
chr16:57912483..57914879hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg382397
hg192397
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472144
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873088
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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