A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863476



Internal ID22638411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42829913..42843235hg38UCSC Ensembl
chr9:44127884..44141206hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3813323
hg1913323
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2117n209
Supporting Variantsnssv17513486, nssv17513487
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863476
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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