A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530985



Internal ID20904346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14799952..15329335hg38UCSC Ensembl
chr20:14780598..15309981hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38529384
hg19529384
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18066688
Samples
Known GenesMACROD2, MACROD2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530985
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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