A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641195



Internal ID21589500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176397451..176397451hg38UCSC Ensembl
chr5:175824452..175824452hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125247
SamplesNA20847
Known GenesCLTB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641195
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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