A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17160878



Internal ID21427990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136074452..136074452hg38UCSC Ensembl
chr9:138966298..138966298hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38480
hg19480
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5641146
Supporting Variants
SamplesHG00731
Known GenesNACC2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17160878
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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