A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641200



Internal ID21589505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:181080301..181080301hg38UCSC Ensembl
chr4:182001454..182001454hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138371
SamplesNA20847
Known GenesLINC00290
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641200
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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