A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116197



Internal ID21467843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37379895..37379950hg38UCSC Ensembl
chr20:36008298..36008353hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592563
Supporting Variants
SamplesHG03125
Known GenesSRC
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116197
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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