A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841108



Internal ID22616043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:130158966..130159965hg38UCSC Ensembl
chr5:129494659..129495658hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494849
Samples
Known GenesCHSY3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841108
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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