A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17442503



Internal ID22500373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86052766..86052766hg38UCSC Ensembl
chr9:88667681..88667681hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5954517
Supporting Variants
Samples
Known GenesGOLM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17442503
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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