A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913582



Internal ID22688798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81615656..81615728hg38UCSC Ensembl
chr9:84230571..84230643hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436382
Samples
Known GenesTLE1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913582
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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