A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551047



Internal ID20924187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27132164..27144559hg38UCSC Ensembl
chr22:27528126..27540520hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3812396
hg1912395
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204952
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551047
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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