A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843826



Internal ID22618761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:9388650..9391524hg38UCSC Ensembl
chr5:9388762..9391636hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg382875
hg192875
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17499573
Samples
Known GenesSEMA5A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843826
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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