A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856534



Internal ID22631469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104059299..104069955hg38UCSC Ensembl
chr9:106821580..106832236hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3810657
hg1910657
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510515
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856534
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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