A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17121329



Internal ID21413893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157121613..157121613hg38UCSC Ensembl
chr3:156839402..156839402hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5611562
Supporting Variants
SamplesHG00513
Known GenesLINC00880
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17121329
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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