A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17098134



Internal ID21476703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88267458..88267458hg38UCSC Ensembl
chr15:88810689..88810689hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5659896
Supporting Variants
SamplesHG03486
Known GenesNTRK3-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17098134
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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