A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873098



Internal ID22648042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10134616..10145225hg38UCSC Ensembl
chr18:10134613..10145222hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3810610
hg1910610
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477103
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873098
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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