A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541734



Internal ID20915011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:29223084..29224541hg38UCSC Ensembl
chr22:29619073..29620530hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg381458
hg191458
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204970
Samples
Known GenesEMID1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541734
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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