A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536869



Internal ID20910213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45306395..45310089hg38UCSC Ensembl
chr22:45702276..45705970hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg383695
hg193695
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205034
Samples
Known GenesFAM118A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536869
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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