A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092635



Internal ID21506063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64431847..64431847hg38UCSC Ensembl
chr15:64724046..64724046hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5646245
Supporting Variants
SamplesNA19983
Known GenesTRIP4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092635
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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