A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17061489



Internal ID21413829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:162720490..162720490hg38UCSC Ensembl
chr1:162690280..162690280hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg382163
hg192163
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5608802
Supporting Variants
SamplesHG00513
Known GenesDDR2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17061489
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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