A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529178



Internal ID20902539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14553045..14654705hg38UCSC Ensembl
chr20:14533691..14635351hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38101661
hg19101661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066960
Samples
Known GenesMACROD2, MACROD2-IT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529178
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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