A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537783



Internal ID20911118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:40907720..40908297hg38UCSC Ensembl
chr21:42279646..42280223hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38578
hg19578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071429
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537783
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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