A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860485



Internal ID22635420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81594569..81597268hg38UCSC Ensembl
chr9:84209484..84212183hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514433
Samples
Known GenesTLE1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860485
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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