A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202177



Internal ID20769217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:13413087..13829468hg38UCSC Ensembl
chr20:13393734..13810114hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38416382
hg19416381
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522420
Supporting Variants
Samples
Known GenesESF1, NDUFAF5, TASP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202177
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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