A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551796



Internal ID20924929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56526316..56536648hg38UCSC Ensembl
chr20:55101372..55111704hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3810333
hg1910333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070418
Samples
Known GenesFAM209B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551796
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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