A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835012



Internal ID22609947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157621408..157625318hg38UCSC Ensembl
chr3:157339197..157343107hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg383911
hg193911
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17486474
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835012
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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