A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640168



Internal ID21588473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179942168..179942168hg38UCSC Ensembl
chr5:179369168..179369168hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131718
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640168
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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