A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090373



Internal ID21487897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35109440..35109440hg38UCSC Ensembl
chr15:35401641..35401641hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5658380
Supporting Variants
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090373
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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