A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828347



Internal ID22603282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150811445..150814475hg38UCSC Ensembl
chr1:150783921..150786951hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg383031
hg193031
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453008
Samples
Known GenesARNT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828347
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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