A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087899



Internal ID21469309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41327735..41327735hg38UCSC Ensembl
chr13:41901871..41901871hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653629
Supporting Variants
SamplesHG03125
Known GenesNAA16
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087899
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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