A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845149



Internal ID22620084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3365122..3366321hg38UCSC Ensembl
chr6:3365356..3366555hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505306
Samples
Known GenesSLC22A23
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845149
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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