A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162436



Internal ID21471575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69379025..69379025hg38UCSC Ensembl
chr9:71993941..71993941hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5632458
Supporting Variants
SamplesHG03125
Known GenesFAM189A2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162436
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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