A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065847



Internal ID20632887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:13970372..13974161hg38UCSC Ensembl
chr20:13951018..13954807hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg383790
hg193790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531634
Supporting Variants
Samples
Known GenesSEL1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065847
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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