A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522332



Internal ID20895693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:133101..204386hg38UCSC Ensembl
chr20:113742..185027hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3871286
hg1971286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065797
Samples
Known GenesDEFB126, DEFB127, DEFB128
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522332
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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