A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516354



Internal ID20889715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:318748..687991hg38UCSC Ensembl
chr20:299392..668635hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38369244
hg19369244
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203263
Samples
Known GenesCSNK2A1, NRSN2, RBCK1, SCRT2, SOX12, SRXN1, TBC1D20, TCF15, TRIB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516354
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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