A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841485



Internal ID22616420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149984280..149986354hg38UCSC Ensembl
chr5:149363843..149365917hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg382075
hg192075
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496280
Samples
Known GenesSLC26A2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841485
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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