A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516679



Internal ID20890040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39449773..39450690hg38UCSC Ensembl
chr20:38078416..38079333hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38918
hg19918
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068900
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516679
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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