A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148719



Internal ID21466076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:101659533..101659533hg38UCSC Ensembl
chr9:104421815..104421815hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642535
Supporting Variants
SamplesHG03065
Known GenesGRIN3A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148719
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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