A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5872926



Internal ID22647868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85604624..85605919hg38UCSC Ensembl
chr16:85638230..85639525hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg381296
hg191296
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17479733
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5872926
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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