A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17070498



Internal ID21490425
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 StatusS
Merged Variantsnsv5631747
Supporting Variants
SamplesNA19238
Known GenesDIP2C, PRR26
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17070498
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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