A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637341



Internal ID21585646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:173891147..173891147hg38UCSC Ensembl
chr5:173318150..173318150hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131716
SamplesHG03683
Known GenesCPEB4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637341
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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