A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089569



Internal ID21491611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83187222..83187222hg38UCSC Ensembl
chr15:83855974..83855974hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5656928
Supporting Variants
SamplesNA19238
Known GenesHDGFRP3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089569
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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