A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5885365



Internal ID22660349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90409786..90413195hg38UCSC Ensembl
chr15:90953018..90956427hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg383410
hg193410
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472392
Samples
Known GenesIQGAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5885365
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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