A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516118



Internal ID20889479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:3490617..3491490hg38UCSC Ensembl
chr20:3471264..3472137hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38874
hg19874
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067976
Samples
Known GenesATRN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516118
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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