A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655865



Internal ID21604170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:45992442..45992442hg38UCSC Ensembl
chr18:43572408..43572408hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101450
SamplesNA19238
Known GenesPSTPIP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655865
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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