A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148882



Internal ID21512815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:974942..1033079hg38UCSC Ensembl
chr8:924942..983079hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3858138
hg1958138
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5672209
Supporting Variants
Samples
Known GenesERICH1-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148882
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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