A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907807



Internal ID22683017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135109842..135110503hg38UCSC Ensembl
chr9:138001688..138002349hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38662
hg19662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430701
Samples
Known GenesOLFM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907807
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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