A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830191



Internal ID22605126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38950343..38953714hg38UCSC Ensembl
chr1:39416015..39419386hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg383372
hg193372
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458015
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830191
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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