A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873771



Internal ID22648719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:57510558..57524924hg38UCSC Ensembl
chr18:55177790..55192156hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3814367
hg1914367
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471370
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873771
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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