A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836764



Internal ID22611699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73806489..73808395hg38UCSC Ensembl
chr3:73855640..73857546hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381907
hg191907
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1461n209
Supporting Variantsnssv17494775, nssv17494776
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836764
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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