A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17085914



Internal ID21449243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95999802..95999802hg38UCSC Ensembl
chr15:96543031..96543031hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646253
Supporting Variants
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17085914
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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