A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541940



Internal ID20915208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:37035911..37036714hg38UCSC Ensembl
chr21:38408211..38409014hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38804
hg19804
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203942
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541940
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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