A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116641



Internal ID21495775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38510613..38510925hg38UCSC Ensembl
chr20:37139256..37139568hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5594659
Supporting Variants
SamplesNA19238
Known GenesRALGAPB
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116641
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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