A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830561



Internal ID22605496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:99835737..99856672hg38UCSC Ensembl
chr1:100301293..100322228hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg3820936
hg1920936
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17481608
Samples
Known GenesAGL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830561
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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