A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610272



Internal ID21558577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:233017335..233017335hg38UCSC Ensembl
chr1:233153081..233153081hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17062937
SamplesHG02011
Known GenesPCNXL2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610272
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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