A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18069047



Internal ID20636087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5012810..5016009hg38UCSC Ensembl
chr20:4993456..4996655hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg383200
hg193200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533607
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18069047
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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