A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159812



Internal ID21498989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133255312..133255312hg38UCSC Ensembl
chr9:136130699..136130699hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5626831
Supporting Variants
SamplesNA19239
Known GenesABO
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159812
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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