A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834708



Internal ID22609643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:149122810..149128108hg38UCSC Ensembl
chr3:148840597..148845895hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg385299
hg195299
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17485664
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834708
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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