A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834656



Internal ID22609591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13123973..13136523hg38UCSC Ensembl
chr3:13165473..13178023hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3812551
hg1912551
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485046
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834656
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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