A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17161758



Internal ID21471690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37034079..37034079hg38UCSC Ensembl
chr9:37034076..37034076hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5629883
Supporting Variants
SamplesHG03125
Known GenesPAX5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17161758
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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