A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224284



Internal ID20791324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135623738..135644416hg38UCSC Ensembl
chr9:138515584..138536262hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3820679
hg1920679
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440981
Supporting Variants
Samples
Known GenesGLT6D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224284
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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