A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553707



Internal ID20926819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:52470023..52479306hg38UCSC Ensembl
chr20:51086562..51095845hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg389284
hg199284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068197
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553707
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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