A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536683



Internal ID20910028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:48179387..48179737hg38UCSC Ensembl
chr22:48575199..48575549hg19UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074692
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536683
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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