A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515780



Internal ID20889141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14821692..14966995hg38UCSC Ensembl
chr20:14802338..14947641hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38145304
hg19145304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4402n223
Supporting Variantsnssv18066727
Samples
Known GenesMACROD2, MACROD2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515780
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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