A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876882



Internal ID22651844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9324114..9327273hg38UCSC Ensembl
chr18:9324112..9327271hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg383160
hg193160
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472620
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876882
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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