A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17121126



Internal ID21496568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41717400..41717400hg38UCSC Ensembl
chr4:41719417..41719417hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5622691
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17121126
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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