A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093338



Internal ID21410364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88267677..88267677hg38UCSC Ensembl
chr15:88810908..88810908hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5648397
Supporting Variants
SamplesHG00512
Known GenesNTRK3-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093338
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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