A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837182



Internal ID22612117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94231867..94236993hg38UCSC Ensembl
chr3:93950711..93955837hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg385127
hg195127
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496892
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837182
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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