A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835563



Internal ID22610498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25020248..25021247hg38UCSC Ensembl
chr3:25061739..25062738hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17490565, nssv17490979
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835563
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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