A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924081



Internal ID22699308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81644735..81645100hg38UCSC Ensembl
chr9:84259650..84260015hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17433509
Samples
Known GenesTLE1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924081
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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