A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116187



Internal ID21462266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37012584..37012660hg38UCSC Ensembl
chr20:35640987..35641063hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600292
Supporting Variants
SamplesHG02818
Known GenesRBL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116187
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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