A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068312



Internal ID21509544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110464574..110464574hg38UCSC Ensembl
chr10:112224332..112224332hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642458
Supporting Variants
SamplesNA20847
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068312
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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