A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116703



Internal ID21456533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46819768..46829535hg38UCSC Ensembl
chr20:45448407..45458174hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg389768
hg199768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590821
Supporting Variants
SamplesHG02492
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116703
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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