A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536480



Internal ID20909827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44928553..44933206hg38UCSC Ensembl
chr22:45324433..45329086hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg384654
hg194654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074478
Samples
Known GenesPHF21B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536480
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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