A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535031



Internal ID20908392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14818827..15134680hg38UCSC Ensembl
chr20:14799473..15115326hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38315854
hg19315854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4386n223
Supporting Variantsnssv18066720
Samples
Known GenesMACROD2, MACROD2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535031
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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