A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152771



Internal ID21494874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96533561..96533561hg38UCSC Ensembl
chr8:97545789..97545789hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5626072
Supporting Variants
SamplesNA19238
Known GenesSDC2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152771
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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