A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540574



Internal ID20913863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:31564070..31564459hg38UCSC Ensembl
chr21:32936383..32936772hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38390
hg19390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071902
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540574
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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