A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613348



Internal ID21561653
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 StatusM
Merged Variants
Supporting Variantsnssv17133576
SamplesHG03125
Known GenesLSG1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613348
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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