A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17133576



Internal ID21471957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194641865..194641865hg38UCSC Ensembl
chr3:194362594..194362594hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5613348
Supporting Variants
SamplesHG03125
Known GenesLSG1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17133576
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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