A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517368



Internal ID20890729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14835124..15098730hg38UCSC Ensembl
chr20:14815770..15079376hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38263607
hg19263607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4386n223
Supporting Variantsnssv18066740
Samples
Known GenesMACROD2, MACROD2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517368
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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