A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832366



Internal ID22607301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201508907..201510341hg38UCSC Ensembl
chr2:202373630..202375064hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg381435
hg191435
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17481979
Samples
Known GenesALS2CR11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832366
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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