A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17069475



Internal ID21435985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17709963..17709963hg38UCSC Ensembl
chr10:17751962..17751962hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5628711
Supporting Variants
SamplesHG00731
Known GenesSTAM
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17069475
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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