A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17154468



Internal ID21494621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:20278025..20278025hg38UCSC Ensembl
chr7:20317648..20317648hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5638317
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17154468
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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