A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17095393



Internal ID21430974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47012294..47012294hg38UCSC Ensembl
chr15:47304492..47304492hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652731
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17095393
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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