A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834966



Internal ID22609901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14548208..14555378hg38UCSC Ensembl
chr3:14589715..14596885hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg387171
hg197171
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485611
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834966
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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