A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532979



Internal ID20906340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38844156..38847764hg38UCSC Ensembl
chr20:37472799..37476407hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg383609
hg193609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068868
Samples
Known GenesPPP1R16B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532979
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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