A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835691



Internal ID22610626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182008244..182013720hg38UCSC Ensembl
chr3:181726032..181731508hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg385477
hg195477
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490372
Samples
Known GenesLOC100996490
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835691
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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