A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526686



Internal ID20900047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14736326..15076563hg38UCSC Ensembl
chr20:14716972..15057209hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38340238
hg19340238
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4386n223
Supporting Variantsnssv18066029
Samples
Known GenesMACROD2, MACROD2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526686
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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