A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835429



Internal ID22610364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:185654309..185674933hg38UCSC Ensembl
chr3:185372097..185392721hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg3820625
hg1920625
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490050
Samples
Known GenesIGF2BP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835429
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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