A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858292



Internal ID22633227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87041528..87052145hg38UCSC Ensembl
chr9:89656443..89667060hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3810618
hg1910618
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514563
Samples
Known GenesLOC440173
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858292
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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