A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626072



Internal ID21574377
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 StatusM
Merged Variants
Supporting Variantsnssv17152771
SamplesNA19238
Known GenesSDC2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626072
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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