A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17117739



Internal ID21512547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63340303..63340497hg38UCSC Ensembl
chr20:61971655..61971849hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598081
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17117739
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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