A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847611



Internal ID22622546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107340153..107342893hg38UCSC Ensembl
chr9:110102434..110105174hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg382741
hg192741
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17510644
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847611
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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