A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545946



Internal ID20919166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:17114014..17127604hg38UCSC Ensembl
chr21:18486332..18499922hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3813591
hg1913591
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203797
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545946
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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