A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878816



Internal ID22653782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37086937..37089436hg38UCSC Ensembl
chr22:37482977..37485476hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1403n209
Supporting Variantsnssv17482931, nssv17482930
Samples
Known GenesTMPRSS6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878816
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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