A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204077



Internal ID20771117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:726662..885250hg38UCSC Ensembl
chr20:707306..865893hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38158589
hg19158588
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6532514
Supporting Variants
Samples
Known GenesANGPT4, FAM110A, SLC52A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204077
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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