A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837096



Internal ID22612031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75097443..75119110hg38UCSC Ensembl
chr3:75146594..75168261hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3821668
hg1921668
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17495334
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5837096
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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