A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657637



Internal ID21605942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88193051..88193051hg38UCSC Ensembl
chr16:88226657..88226657hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089418
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657637
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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