A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834261



Internal ID22609196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109165072..109199615hg38UCSC Ensembl
chr3:108883919..108918462hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3834544
hg1934544
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17483693
Samples
Known GenesLINC00488
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834261
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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