A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145585



Internal ID21421409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:58993880..58993880hg38UCSC Ensembl
chr8:59906439..59906439hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5632712
Supporting Variants
SamplesHG00731
Known GenesTOX
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145585
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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