A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841197



Internal ID22616132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:153324120..153331161hg38UCSC Ensembl
chr5:152703680..152710721hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg387042
hg197042
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496327
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841197
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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