A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17069218



Internal ID21482962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15071243..15071243hg38UCSC Ensembl
chr10:15113242..15113242hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5625839
Supporting Variants
SamplesHG03732
Known GenesOLAH
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17069218
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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