A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555123



Internal ID20928212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16773501..16774600hg38UCSC Ensembl
chr21:18145820..18146919hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203794
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555123
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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