A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17133693



Internal ID21486816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158245131..158245131hg38UCSC Ensembl
chr3:157962920..157962920hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5613839
Supporting Variants
SamplesNA12878
Known GenesRSRC1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17133693
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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