A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067296



Internal ID20634336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39707631..39707945hg38UCSC Ensembl
chr20:38336273..38336587hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553443
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067296
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00112


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