A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5835999



Internal ID22610934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44867320..44868519hg38UCSC Ensembl
chr3:44908812..44910011hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17491547
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5835999
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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