A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17115973



Internal ID21454593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32123203..32123203hg38UCSC Ensembl
chr20:30711006..30711006hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670918
Supporting Variants
SamplesHG02011
Known GenesTM9SF4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17115973
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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