A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17115913



Internal ID21505652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23735659..23811500hg38UCSC Ensembl
chr20:23716296..23792137hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3875842
hg1975842
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601271
Supporting Variants
SamplesNA19650
Known GenesCST1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17115913
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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