A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230506



Internal ID20797546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86052921..86053838hg38UCSC Ensembl
chr9:88667836..88668753hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38918
hg19918
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448888
Supporting Variants
Samples
Known GenesGOLM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230506
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.04312


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