A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834812



Internal ID22609747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180681192..180683158hg38UCSC Ensembl
chr3:180398980..180400946hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg381967
hg191967
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489733
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834812
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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