A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530416



Internal ID20903777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:9916442..9924641hg38UCSC Ensembl
chr20:9897090..9905289hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg388200
hg198200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069265
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530416
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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