A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837469



Internal ID22612404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94818387..94848520hg38UCSC Ensembl
chr3:94537231..94567364hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3830134
hg1930134
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497475, nssv17492184
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837469
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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