A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704763



Internal ID21377039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135109843..135110504hg38UCSC Ensembl
chr9:138001689..138002350hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38662
hg19662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4389194
Supporting Variants
Samples
Known GenesOLFM1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704763
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0201149


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