A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631747



Internal ID21580052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:657527..657527hg38UCSC Ensembl
chr10:703467..703467hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38744
hg19744
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070498
SamplesNA19238
Known GenesDIP2C, PRR26
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631747
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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