A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908028



Internal ID22683238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109769070..109769122hg38UCSC Ensembl
chr9:112531350..112531402hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17444560
Samples
Known GenesPALM2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908028
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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