A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536622



Internal ID20909968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38644816..38650830hg38UCSC Ensembl
chr22:39040821..39046835hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg386015
hg196015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073988
Samples
Known GenesFAM227A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536622
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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