A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828036



Internal ID22602971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154657074..154689907hg38UCSC Ensembl
chr1:154629550..154662383hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3832834
hg1932834
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17452311
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828036
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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