A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17096000



Internal ID21465883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41978067..41978067hg38UCSC Ensembl
chr15:42270265..42270265hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662193
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17096000
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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