A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159716



Internal ID21479195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121327716..121327716hg38UCSC Ensembl
chr9:124089994..124089994hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5628290
Supporting Variants
SamplesHG03486
Known GenesGSN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159716
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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