A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17107406



Internal ID21498407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:100037436..100037436hg38UCSC Ensembl
chr2:100653898..100653898hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5619761
Supporting Variants
SamplesNA19239
Known GenesAFF3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17107406
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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