A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17096091



Internal ID21479806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31290891..31290961hg38UCSC Ensembl
chr17:29617909..29617979hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590365
Supporting Variants
SamplesHG03486
Known GenesNF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17096091
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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