A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5912832



Internal ID22688048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107487627..107487677hg38UCSC Ensembl
chr9:110249908..110249958hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448137
Samples
Known GenesKLF4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5912832
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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