A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537527



Internal ID20910861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36409802..36418406hg38UCSC Ensembl
chr22:36805847..36814451hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg388605
hg198605
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204616
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537527
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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