A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828050



Internal ID22602985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157984245..157988869hg38UCSC Ensembl
chr1:157954035..157958659hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg384625
hg194625
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457977
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828050
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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