A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17117781



Internal ID21452845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63919438..63919661hg38UCSC Ensembl
chr20:62550791..62551014hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38224
hg19224
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5587639
Supporting Variants
SamplesHG02011
Known GenesDNAJC5, MIR941-1, MIR941-3, MIR941-4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17117781
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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