A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17091741



Internal ID21478483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32506926..32506926hg38UCSC Ensembl
chr13:33081063..33081063hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5657506
Supporting Variants
SamplesHG03486
Known GenesN4BP2L2, N4BP2L2-IT2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17091741
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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