A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065850



Internal ID20632890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14016501..14018400hg38UCSC Ensembl
chr20:13997147..13999046hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515969
Supporting Variants
Samples
Known GenesMACROD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065850
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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