A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17119267



Internal ID21453284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:29762668..29762668hg38UCSC Ensembl
chr21:31134987..31134987hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665321
Supporting Variants
SamplesHG02011
Known GenesGRIK1, GRIK1-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17119267
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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