A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17140982



Internal ID21440930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:114997018..114997067hg38UCSC Ensembl
chr8:116009247..116009296hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5583481
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17140982
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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