A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18066957



Internal ID20633997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14532149..14615660hg38UCSC Ensembl
chr20:14512795..14596306hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3883512
hg1983512
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527658
Supporting Variants
Samples
Known GenesMACROD2, MACROD2-IT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18066957
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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