A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850122



Internal ID22625057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102695291..102700716hg38UCSC Ensembl
chr13:103347641..103353066hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg385426
hg195426
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459115
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850122
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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