A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553330



Internal ID20926438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42015338..42016027hg38UCSC Ensembl
chr21:43435447..43436136hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38690
hg19690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071573
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553330
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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