A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864972



Internal ID22639907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32316983..32344461hg38UCSC Ensembl
chr9:32316981..32344459hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3827479
hg1927479
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17512953
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864972
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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