A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523941



Internal ID20897302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38867017..38879394hg38UCSC Ensembl
chr20:37495660..37508037hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3812378
hg1912378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068870
Samples
Known GenesPPP1R16B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523941
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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