A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17059947



Internal ID21476569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111607657..111607657hg38UCSC Ensembl
chr1:112150279..112150279hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38254
hg19254
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5607603
Supporting Variants
SamplesHG03486
Known GenesLOC100129269
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17059947
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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