A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835684



Internal ID22610619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177935718..177938367hg38UCSC Ensembl
chr3:177653506..177656155hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg382650
hg192650
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490018
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835684
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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