A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645947



Internal ID21594252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56739342..56739342hg38UCSC Ensembl
chr16:56773254..56773254hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17092512
SamplesHG02011
Known GenesNUP93
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645947
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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