A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5873701



Internal ID22648649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37093704..37095773hg38UCSC Ensembl
chr22:37489744..37491813hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg382070
hg192070
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17482932
Samples
Known GenesTMPRSS6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5873701
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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