A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084887



Internal ID21467487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32816234..32816234hg38UCSC Ensembl
chr13:33390372..33390372hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg386067
hg196067
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662165
Supporting Variants
SamplesHG03065
Known GenesLINC00423
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084887
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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