A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17140295



Internal ID21487576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:58006923..58006923hg38UCSC Ensembl
chr8:58919482..58919482hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5628074
Supporting Variants
SamplesNA18534
Known GenesFAM110B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17140295
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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