A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17070499



Internal ID21490424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:657836..657836hg38UCSC Ensembl
chr10:703776..703776hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5635674
Supporting Variants
SamplesNA19238
Known GenesDIP2C, PRR26
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17070499
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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