A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865776



Internal ID22640711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99436039..99440265hg38UCSC Ensembl
chr13:100088293..100092519hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg384227
hg194227
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452988
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865776
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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