A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834367



Internal ID22609302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150916249..150925239hg38UCSC Ensembl
chr3:150634036..150643026hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg388991
hg198991
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485682
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834367
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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