A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17082725



Internal ID21457967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96400637..96400637hg38UCSC Ensembl
chr15:96943867..96943867hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38988
hg19988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5656922
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17082725
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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