A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549618



Internal ID20922780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:22135494..22320307hg38UCSC Ensembl
chr21:23507814..23692627hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38184814
hg19184814
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205960
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549618
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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