A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830361



Internal ID22605296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:5112556..5115261hg38UCSC Ensembl
chr1:5172616..5175321hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg382706
hg192706
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480493
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830361
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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