A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202567



Internal ID20769607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2603189..2656563hg38UCSC Ensembl
chr20:2583835..2637209hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3853375
hg1953375
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527105
Supporting Variants
Samples
Known GenesMIR1292, NOP56, SNORA51, SNORD110, SNORD86, TMC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202567
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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