A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873259



Internal ID22648204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28605308..28609994hg38UCSC Ensembl
chr16:28616629..28621315hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg384687
hg194687
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17469893, nssv17477734, nssv17477735, nssv17469892
Samples
Known GenesSULT1A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873259
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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