A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204626



Internal ID20771666
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 StatusS
Merged Variantsnsv6545738
Supporting Variants
Samples
Known GenesTMPRSS6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204626
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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