A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610880



Internal ID21559185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2221917..2221917hg38UCSC Ensembl
chr4:2223644..2223644hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38621
hg19621
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128854
SamplesNA20509
Known GenesPOLN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610880
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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