A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914872



Internal ID22690089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81612979..81613064hg38UCSC Ensembl
chr9:84227894..84227979hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436261
Samples
Known GenesTLE1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914872
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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