A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549425



Internal ID20922587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39351957..39361284hg38UCSC Ensembl
chr21:40723883..40733210hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg389328
hg199328
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203959
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549425
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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