A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536823



Internal ID20910166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11463001..11464600hg38UCSC Ensembl
chrUn_gl000233:34945..36544hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071579
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536823
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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