A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092839



Internal ID21484334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40374014..40374014hg38UCSC Ensembl
chr15:40666215..40666215hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663896
Supporting Variants
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092839
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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