A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835108



Internal ID22610043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:171376639..171381846hg38UCSC Ensembl
chr3:171094428..171099635hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg385208
hg195208
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489641
Samples
Known GenesTNIK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835108
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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