A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657588



Internal ID21605893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:397709..397709hg38UCSC Ensembl
chr16:447709..447709hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38865
hg19865
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094110, nssv17085196
SamplesNA19238, HG00732
Known GenesNME4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657588
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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