A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17130573



Internal ID21414836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53578919..53578919hg38UCSC Ensembl
chr4:54445086..54445086hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5610406
Supporting Variants
SamplesHG00513
Known GenesLNX1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17130573
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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