A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17136050



Internal ID21449918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:45080116..45080116hg38UCSC Ensembl
chr4:45082133..45082133hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5606744
Supporting Variants
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17136050
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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