A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17099222



Internal ID21485127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73610459..73610459hg38UCSC Ensembl
chr13:74184596..74184596hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646402
Supporting Variants
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17099222
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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