A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17070126



Internal ID21484560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:322878..322878hg38UCSC Ensembl
chr10:368818..368818hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg381937
hg191937
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5640627
Supporting Variants
SamplesNA12329
Known GenesDIP2C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17070126
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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