A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528237



Internal ID20901598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:11096307..11097089hg38UCSC Ensembl
chr20:11076955..11077737hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38783
hg19783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066286
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528237
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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