A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526147



Internal ID20899508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14652702..14909292hg38UCSC Ensembl
chr20:14633348..14889938hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38256591
hg19256591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4381n223
Supporting Variantsnssv18066010
Samples
Known GenesMACROD2, MACROD2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526147
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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