A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084915



Internal ID21502960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86336703..86336703hg38UCSC Ensembl
chr16:86370309..86370309hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5656594
Supporting Variants
SamplesNA19239
Known GenesLINC00917
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084915
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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