A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080583



Internal ID21480480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:138346..138407hg38UCSC Ensembl
chr16:188345..188406hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603194
Supporting Variants
SamplesHG03683
Known GenesNPRL3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080583
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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