A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644737



Internal ID21593042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66474544..66474544hg38UCSC Ensembl
chr16:66508447..66508447hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17083775
SamplesHG03371
Known GenesBEAN1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644737
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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