A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537665



Internal ID20911000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:21836509..21867856hg38UCSC Ensembl
chr21:23208829..23240176hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3831348
hg1931348
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205954
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537665
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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