A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539725



Internal ID20913020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40171459..40176362hg38UCSC Ensembl
chr22:40567463..40572366hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg384904
hg194904
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073811
Samples
Known GenesTNRC6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539725
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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