A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515719



Internal ID20889080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14623304..14851566hg38UCSC Ensembl
chr20:14603950..14832212hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38228263
hg19228263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4381n223
Supporting Variantsnssv18066004
Samples
Known GenesMACROD2, MACROD2-IT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515719
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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