A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17117979



Internal ID21447467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62954025..62954077hg38UCSC Ensembl
chr20:61585377..61585429hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586179
Supporting Variants
SamplesHG00732
Known GenesSLC17A9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17117979
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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