A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092512



Internal ID21453546
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 StatusS
Merged Variantsnsv5645947
Supporting Variants
SamplesHG02011
Known GenesNUP93
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092512
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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