A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090168



Internal ID21999401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137102931..137102931hg38UCSC Ensembl
chr9:139997383..139997383hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583830
Samples
Known GenesMAN1B1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6090168
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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