A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17142140



Internal ID21477001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89099413..89099413hg38UCSC Ensembl
chr6:89809132..89809132hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639261
Supporting Variants
SamplesHG03486
Known GenesSRSF12
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17142140
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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