A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527105



Internal ID20900466
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 StatusM
Merged Variants
Supporting Variantsnssv18202567
Samples
Known GenesMIR1292, NOP56, SNORA51, SNORD110, SNORD86, TMC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527105
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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