A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555489



Internal ID20928576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16563244..16563950hg38UCSC Ensembl
chr21:17935564..17936270hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38707
hg19707
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203790
Samples
Known GenesLINC00478
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555489
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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