A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545230



Internal ID20918463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43717701..43719400hg38UCSC Ensembl
chr21:45137582..45139281hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204115
Samples
Known GenesPDXK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545230
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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