A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067567



Internal ID21502984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11742311..11742311hg38UCSC Ensembl
chr10:11784310..11784310hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5630581
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067567
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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