A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863511



Internal ID22638446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135178769..135181868hg38UCSC Ensembl
chr9:138070615..138073714hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511772
Samples
Known GenesLOC401557
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863511
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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