A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545738



Internal ID20918964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37087194..37096386hg38UCSC Ensembl
chr22:37483234..37492426hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg389193
hg199193
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204626
Samples
Known GenesTMPRSS6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545738
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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