A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17133743



Internal ID21506700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183823908..183823908hg38UCSC Ensembl
chr4:184745061..184745061hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5632629
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17133743
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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