A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828074



Internal ID22603009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161988328..162023699hg38UCSC Ensembl
chr1:161958118..161993489hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3835372
hg1935372
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457010
Samples
Known GenesOLFML2B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828074
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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