A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517173



Internal ID20890534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1899181..1902457hg38UCSC Ensembl
chr20:1879827..1883103hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg383277
hg193277
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067332
Samples
Known GenesSIRPA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517173
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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