A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546858



Internal ID20920068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50190601..50193700hg38UCSC Ensembl
chr20:48807138..48810237hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18069056
Samples
Known GenesCEBPB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546858
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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