A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589693



Internal ID21781736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137103097..137103097hg38UCSC Ensembl
chr9:139997549..139997549hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6089909
Supporting Variants
Samples
Known GenesMAN1B1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589693
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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